Some standard content:
Health Industry Standard of the People's Republic of China
ws/t 203-2001
Standard terminolugy for blood transfusion medicine
Published on 2001-07-20
Published by the Ministry of Health of the People's Republic of China
2002 -01-01 Implementation
WS/T203-2501
Management technical system
Selection of blood donation provinces
Blood donors' inspection
Blood collection
Blood component preparation
Labeling and barcoding
Storage, transportation and validity period
Blood type matching
Clinical establishment
Blood transfusion complications
Leukocyte accumulation
Glucose deficiency and blood coagulation
WS/R273-2001
After checking the blood collection methods and corresponding standards, The formulation of transfusion medicine terminology standards is a first step. This standard is mainly selected from the blood test industry at home and abroad. The World Health Organization's biological standards, the World Health Organization's blood test standards, and the World Health Organization's blood test standards are published in the 17th edition (19). The standard is composed of definitions, annotations, and other parts of the above publications. The rest of the standard is self-extracted. Blood medicine was originally a branch of medical treatment. In modern times, it has integrated many high-tech and developed into a professional discipline. The terminology of blood transfusion medicine is becoming increasingly rich. As the first edition of the blood transfusion medicine field, it is difficult to include all the terms. This standard only gives priority to the commonly used auxiliary blood medicine terms.
This standard is the technical basis of the blood transfusion medicine profession. It is the basis for the formulation of technical standards, management standards and related evidence for the medical profession. This standard is the technical method for the use of blood medicine in the blood transfusion medicine profession. The selection of terms in various related disciplines is limited. Each related discipline can refer to the terminology standards of this discipline. This standard shall be effective from January 1, 2502. The standard shall be issued by the Ministry of Health. The drafting unit of the standard is Shanghai Blood Center. The drafters are Liu Qiuyuan, Zhang Gongliang, Zhang Yinduan, Li Xiaoxun and Yu Yongding. This standard shall be interpreted by the Ministry of Health and the China Transfusion Association. 1. Standard of Health Industry of the People's Republic of China
Common Terminology of Blood Transfusion Medicine
Standard lermlnology far hlaad transfusion mcdicine This standard defines the standardized terms and their meanings of commonly used management and technical terms in transfusion medicine. This standard is applicable to the reference and interpretation of transfusion medicine and related fields to transfusion medical manuals. 2. The following definitions must be adopted in this standard.
2.1 Transfusion MedicineIrunsfusiunmedielnew$/T203—2001
It is an independent discipline in medical science that studies topics related to clinical transfusion therapy. Its main research objects are: blood collection and supply and its management, collection and management of blood substitutes, blood sample collection and testing, preparation and quality control of blood components, blood type and blood matching, HIA typing and tissue compatibility test, separation and storage of peripheral blood containing blood stem cells and blood samples, development of blood substitutes, transfusion indications and various component matching, autologous blood supplementation, therapeutic blood collection, weak positive correlation according to the disease phase of transfusion complications and their prevention, etc. 2.2 Blood songbluud
Total blood and component blood used in clinical practice:
Blood donationbluud
To help the dying and the wounded, it is a noble act of self-donation. 2.4 Blood transrusion
The process of safe and effective blood transfusion according to the actual needs of the patient. 3 Management termsWww.bzxZ.net
3.1 Blood donation management
3.1.1 Blood donation law
law of blood donation
The term for the Blood Donation Law of the People's Republic of China, a legal document formulated by the competent authority to issue blood donation laws and regulations, including the purpose, management principles and law enforcement basis of blood donation work.
2 Blood donation regulations The series of guiding documents on management and technology and local relevant laws and regulations issued frequently by the health administration department of the State Council for the implementation of the Blood Donation Law of the People's Republic of China,
Blood planning
Based on the population, industrial structure, medical institution settings and scale of the region, the estimation of the short-term and long-term blood supply and demand, and the planning of blood source collection and medical use. 3.1.4 Blood resource management management or blood resources local people's governments at all levels oversee the organization, coordination and coordination of blood donation work in their respective regions and cities
3.1.5 Blood circulation blood circulation systems
Ministry of Health of the People's Republic of China 20-07-20 approved 2002-01-01 implementation
warm blood normal health people
WS.T 203 2001
31.f wheel two hlodiraosfaslonadministration good law clinical blood seal, maintenance and some clinical price blood cross-hospital pre-renal management monitoring sales 3. 1. 7 clinical blood lmcl Tr rtimirl ust clinical treatment of whole blood, wave separation in blood waiting for light general term. $1. No # remember cerrificalefnrvulunieerooddnatin school! Department of Health: preparation, training, record and donation of blood. 3.2 Public blood collection institutions
3.2.1 Blood stations
are non-profit institutions that provide blood for the public benefit of the public. 3.23
A blood station is a blood station approved by the Ministry of Health of the People's Republic of China in the capital city of a province, autonomous region or prefecture-level city of a city. 2.2.3 A blood station is a blood station approved by the health administration department of the State Council in a city, a provincial capital city, an autonomous region or prefecture-level city, a district or a district. 3.2.4 A blood station is a blood station approved by the health administration department of a county or a district. 3.2.5 Central blood bank A blood bank is a blood donation point approved by the provincial health administration department and is responsible for the blood supply of blood. 3.2.6 Blood donation points A blood donation point (room) in the region approved by the local health administration department and is responsible for blood screening, blood matching and blood diagnosis and treatment. 3.2.8 Plasma stations are only for the expansion of blood products and do not collect and supply blood products. 3.3 Blood station quality management 33.1 Blood management quality management is sure to love products! , and in the quality system through the quality system, such as quality control, quality assurance and quality improvement to achieve your full management requirements.
3.3? Policy quliyprliry
The overall quality and quality direction of the group planner. 3.3.3 Quality Controlyuliyeuarul
To meet the requirements of the project, quality assurancequalityaksurance
In order to be able to show that the entity can meet the quality requirements, the system activities that need to be verified in the system are implemented in the system.||tt ||3.3-5 Blood station quality management specifications (CMP) blood station quality management system ...8 Blood safety bluudsafrly
WS/T203—200T
The risk of blood recipients and related persons is limited to the safe level of blood recipients. 3- 3.9 Blood injection effectiveness bilvod lldity Under the standard blood injection strips. Blood injection efficacy needs to be sufficient for clinical treatment. 3.4 Records
3.4.1 Blood station records Ilond trasfusinll serrice rernrds anti-blood station reception and technical work to implement the standard actual situation of blood flow report standardization, 3.4.2 Blood source record blood record 3.4.3 Confidentiality of records for records The blood station shall record whether the blood donation is released, the name of the blood recipient or his family members and the privacy of the individual. 3.4.4 Record-keeping system The blood station shall maintain the collection, sorting, return, storage and deactivation systems and technical systems 4. Selection of blood donors
4.1 Blood donors
4.1.1 4.1.3 Unpaid blood donors Blood donors who do not seek financial compensation. 4.1.4 Paid blood donors Blood donors who receive financial compensation 4.1.5 Standard blood donors Health examination standards for blood donors. 4.1.6 Micro-blood card card for blood donation indicates whether the blood donor has been compliant with the regulations of the health administration department of the Ministry of Health on the health conditions of blood donors. 4.2 History of viral hepatitis History of viral hepatitis The history of the blood donor and the patient's health status according to the prescribed consultation items. 4.2.2 History of viral hepatitis History of viral hepatitis The history of liver pathological changes caused by infectious diseases: The viruses that can cause hepatitis mainly include hepatitis B virus, ... 4.2.5 Parenteral drugs 5 Drugs that are used by other than the parenteral route of administration 5 or blood test 5. Hemoglobin 5. Hemoglobin: copper sulfate method W8/T203:20C1 A method for determining the lower limit of hemoglobin concentration in non-concentrated aqueous solution (eg, hemoglobin acid) A 1.1. 5.1.2 Hemoglobin concentrations: henioglobinometry Hemoglobin concentration in concentrating blood samples Aphlursmethad Por hematacrlt assay 5. 1.2 Capillary flow cytometry: The blood sample is centrifuged at a required density and the volume is measured to calculate the hemoglobin content. 5.2 Infectious Disease Screening: h.2.1 Infectious Disease Screening: Blood samples of donors can be tested and identified for infectious diseases as specified by the country. 5.2.2 Infectious Disease Screening: The general term for infectious disease pathogens, antigens, and other infectious phenomena detected in the blood, as well as surrogate test materials. Suogalestiog
A non-specific biomarker of the rapid acquisition of the body and the test: the replacement of the note can indicate the presence of pathogens, but it is not a specific marker of the pathogen infection.
A metastatic hepatitis B is a kind of hepatitis B virus that exists in cells such as the liver and the moon. Cell damage caused by various reasons can lead to an increase in its content in the body. Hepatitis B surface antigen.HlBxAp5.2. 5
Hepatitis B virus antibody is one of the markers of hepatitis B virus infection. 5.2.GZ Hepatitis B virus antibody antibodlestahepatlilsBcore.anti-HBc is a relative antibody of hepatitis B virus nucleus. 5.2.? Hepatitis C virus antibody nntibudiesluhetilisviru>.mni-HCy machine anti-viral antibody against hepatitis C virus infection. A marker of hepatitis C virus infection 5.2.8 Human immune deficiency virus antibody antihadieskhumanimmunodeficiencyvlrus.anti-Hiy machine anti-human immunodeficiency virus infection antibody, a marker of human immunodeficiency virus infection. 5.2. 9
syphilis plasma test syphilisplasmarcagin loss of blood and the United States are all non-specific reagents protein juice: Ya can not, leprosy, blood scar and other blood can be caused by the heart of the fee type criminal army collection 57.10 linked immune test rnzvm: linkedimmunvsurbentassey.EL15A based on the principle of immunology to pull the original antibody to hold the different platform. Enzyme labeling or antigen, the corresponding amplification or antibody about the elimination method. 5. 2.11
protein blotting method westernbin
on the carrier printed with purified antibody electrophoresis rapid, the corresponding antibody method. In the detection of transfusion-transmitted diseases, it is used as a test method for the identification of human immune antibodies. 5.2.12 Recombinant immunoblot ssay, KIBA uses recombinant antibodies to transfer to the body and detect the corresponding antibodies. In the detection of blood-transmitted diseases, it is a more sensitive and effective method for detecting antibodies to hepatitis B virus. 5.2.13 Rapid plasma reaglin test. RPR￥5/T203—2001
It uses synthetic lipids as the main raw material and reagents to absorb carbon dioxide. It is a rapid method for detecting hepatitis B virus reagin. 5-2.14 Hemagglutination test. Rhitis spinillum antibody hemoagglutination test. A method for detecting the reconciliation of red blood cells sensitized with a specific antigen to detect the corresponding antibodies. 5.2.15 Optical density 0.D photoelectric colorimetric reading value of the specific light intensity under hazardous conditions. 5.2.16 Limit value eul ufrvall
determinative or negative limit,
confirmatory testcnntirmatarytest
for a product that shows a positive or negative reaction early, it is necessary to use an accurate and reliable fluorescent technique to further confirm the test,
5.2.18 positive
test means the test shows a positive result, such as: in the infectious disease selection report, it means that the infectious disease marker has been detected, 5.7.19 positive
test means the negative result of the test. For example: in the infectious disease benefit report, it means that the infectious disease marker has been detected, 5-2-20
can indeterminate
the test result is not determined as positive, nor can it be judged as negative. 5. 2.21
false positive
negative samples, those tested positive,
false negative
positive products, suspected
first testing
testing
testing blood samples collected from blood donors during health check-up, 5.2.24 retesting
testing blood samples collected from blood donors during blood donation, 5.2.25 repeat testing
testing blood samples that test positive or are inaccurate. 5.3 Screening laboratory quality control
5.3.? Indoor medical control laboratory acceptance and technical actions taken to ensure the accuracy of test data. 5.3.2 Specificity
The minimum value of the detection target of a reagent or test method 5.3.3 Specificity
The possibility of detecting a qualitative reaction in an individual infected with a certain pathogen. 5.3.4 Quality control serum Quality control serum The reference serum used for indoor or laboratory quality control to maintain the constant quality of the test object under specified conditions 5.3.5 Conditional variation
The best level of precision that can be achieved for a test item under the same experimental conditions 5.3.6 Routine conditionriantt, RC The level of precision variation for a test item in the routine work of the same laboratory 5.3.7 Error
The difference between the measured value and the actual or expected value. 5. Quality management and evaluation of the units or laboratories approved by the competent authority, and the monitoring and evaluation of the quality of the inspection of the whole medical or industry laboratory. 6. Blood case continuation
6 1 Case points
6.1.1 Confirm the blood donor's identity, the name of the blood donor and the blood replacement label, blood type, blood donation number and other items during the blood collection process: 6-1.2 The anterior area of the anterior area is the upper part of the anterior area of the anterior area, and the vein is not usually injected with blood. 6.1.3 Supply indinc tineture
Monthly skin toxicity, please and 1.: The ethanol concentration is about 2 times. E.1.4 Blood hhdbag
Blood collection, distribution, storage, transportation and injection of plastic bags hloideallectinghsg
Non-blood collection needle. Case blood guide can be suitable for early anticoagulant container. Used for blood collection of about fully sealed plastic containers. 5. :. 6 Transfer hae
Catheter Li Wang space device composed of blood components, preparation, preservation of blood components of the whole patient sealed material container. 5-1.7 Collection point hlrud cnlleetion
State of age of blood collection of embryonic blood in the container. 5. B whole blood whnle hlnnd
Record human blood container appropriate anticoagulant deduction of three percent of each blood component. 61.9 positive liquid) unit (ood) n
Name of blood, with 2 heart. Whole unit. 6.2.1 Aseptic procedure refers to the process of sterilization of any component of a single unit. The sterilization procedure refers to the process of sterilization of any component of a unit. The sterilization procedure refers to the process of sterilization of any component of a unit. The sterilization procedure refers to the process of sterilization of any component of a unit. The sterilization procedure refers to the process of sterilization of any component of a unit. The sterilization procedure refers to the process of sterilization of any component of a unit. The sterilization procedure refers to the process of sterilization of any component of a unit. The sterilization procedure refers to the process of sterilization of any component of a unit. The sterilization procedure refers to the process of sterilization of any component of a unit. The sterilization procedure refers to the process of sterilization of any component of a unit. The sterilization procedure refers to the process of sterilization of any component of a unit. The sterilization procedure refers to the process of sterilization of any component of a unit. The sterilization procedure refers to the process of sterilization of any component of a unit. The sterilization procedure refers to the process of sterilization of any component of a unit. E.2.7 Sterile dispasable syringes are matched with injection devices, and are non-pyrogenic and non-packaging. Disposable syringes are 62.8 Clean area cleanareas
Areas composed of clean and fresh air.
E.2.9 Clean room lean rm
A studio that meets the requirements of process specifications for cleanliness, blueness, certification, pressure difference, air volume and media, 6.2.10 Cleanliness leanllhes8
The degree of air content and actual volume in the clean circulation, purification purificnti
w$1 203—2001
The process of removing pollutants under pressure to achieve a certain cleanliness, 6-2.12 Air purification Arpurification The air cleanliness of the purification area, the air passages and directions should be lightly controlled. 6.2.13 Personnel purification workerclenming The sanitation purification process of the staff before entering the clean room. 6.2.14
Wind shower
Strong wind blows away the dust particles on the surface of the personnel and materials. 6.2.15
The route that the staff moves during the operation according to the process flow requirements, the logistics flow
The route that the staff moves according to the process flow requirements. 6.3 Anticoagulants
6.3. Anticoagulants
Substances or culture materials that prevent blood loss
6.3.2 Acp-B acid citratedextroseBsolutlon blood anticoagulant and preservation compound sodium phosphodiesterase, CPD solution ehtrate phosphele dexirose soluliun6.3. 3
Blood anticoagulation and preservation containing acid, iodine, phosphate, oxygen, sodium and bacteria, 6-3.4 CrD-A solution citrate phesphate dexrrose adenlne solutlon blood swab and preservation ear gland noise dong C sanitary solution CP2D*ehtrutephhsphale2dexlrusyolutiun6. 3.5
Blood transfusion CP formula with reduced content, Cr2D- cltrate plesphate 2 dextrose adeninc solulion6- 3. 6
Blood supplement with cold 21) standard,
64 Du reaction
6.4.1 Blood donation adverse donation reartinns use general point cause human physiological or pathological abnormal reaction, 6-4.2 Blood transfusion care the careaf blwod The consultation, environment, safety and medical monitoring services provided by the donors. 6.4.3 Hermalama
The blood donation caused by the puncture is a single piece of blood on the skin. 6.4.4 Vascular vasovagal symptoms that occur during blood collection, such as: hyperthermia, rapid heartbeat and breathing, pale face with redness, dizziness, nausea or vomiting, etc., in the blood donor. 5. Dose sensitivity raint
State start blood loss and loss of consciousness. 6.4.6 Recovery unyulsiuns
Manifested as involuntary contraction or tonic tension of the quadriceps, lower back and forehead and facial storage muscles, accompanied by related motor and cognitive reactions.
6.4.7 Hyperventilation Respiratory syndrome caused by static ventilation of more than 1 heart per minute in adults, occasionally seen in blood donors with hyperventilation. Manifested as a change in the sense of emergency
6.4.8 Accidelinjur?
WN.T203-20C1
Total material loss caused by the return difference, such as: blood donation old four fainting price or new retention method caused by the damage 6.4.5 Air embolism room iremlalisrn
Angry people Sa ball caused by blood flow obstruction set
6.4.10. Phlebliis
Partial swelling, heat, pain and other symptoms. ! Preparation of blood components
7.1 Blood and plasma
Red blood cellsredhldcells
The blood contains large nuclei, hemoglobin, H2O2 and some red blood cells that need oxygen. 7.2 Platelets
Platelets are small and irregular in shape, and are formed elements involved in blood analysis or preparation. 7.3 Granulocytes
A group of white blood cells contained in the blood plasma and neutrophils. 7.1 Plasma
The liquid part of blood, which carries blood factors and other substances such as white blood cells, blood factors and chemicals. 7.2 Blood component preparation
7. 2, 1 Blood components are the general term for various three-liquid component products prepared by dividing blood into two parts. 7. 2. 2 Whole blood components are whole blood that meets the requirements for preparing blood components.
7.2.3 Centrifugal separation
The process of separating blood of all densities by centrifugal force. 7.2.4 Buffer coal layer
The white membrane-like layer between the plasma layer and the solid layer after centrifugation or natural precipitation, which contains platelets and granulocytes.
7.2.5 Cell layer llulst Praron
The dark red layer mainly composed of leukocytes is the lower layer after whole blood is separated or naturally precipitated. 7.2.5 Washing
The process of removing almost all plasma from whole blood. 7.2.7
The process of removing leukocytes from concentrated whole blood by passing through a leukocyte remover. 7.2. The process of transferring certain components within a sealed separation system is as follows: 7.3 Red blood cell components 7.3.1 Concentrated red blood cells Removing most of the plasma and reducing the red blood cell volume. 7.3.2 Suspended red blood cells Add a certain amount of red blood cell suspension to the red blood cell component of the corresponding red blood cell type. 7.3.3 Reduced autoimmune red blood cell components Retain at least 50% of the red blood cell components below the standard of whole blood and reduced leukocyte count. Sweat: To prevent fever and convulsions, the amount of white blood cell in the product should be less than 11.4 times the amount of 100mg/ml of water. The amount of water should be less than 5X1WST 203291
7.3. 4 Washing red blood cells
remove almost all blood and most of the high red blood cell content of the blood cells 7.3.5 Freezing lamp plastic cells fro2enredbloodcells busy in the ice refining forest, after the high red blood cell content of the washing stone, Shengdao red Yi brittle irrndiatedredbludrells7. 3.6 4
after 250C:y~000Gy radiation dose of red blood cell components: 7.3./Rejuvenated red blood cell purchase rejuvenated The red blood cells that have expired for one day at 2--C are restored to the level of 2.3-phosphoglyceraldehyde 1 (2.3->PG) and triglyceride (ATH) by the method of the left method. 7.4 Plasma components
7.4.1 Fresh frozen plasma treshfranplHsFFF is a single plasma that is stored below -18 within 5 days after blood collection. Note: Alpine plasma is separated within 24 hours after blood collection. Quick-frozen plasma that is not stored below -18 is separated within 24 hours after blood collection. 7.4.3 Frozen plasma, RhP is separated within one week after blood collection and stored below -13°C. 7.4.4 Cryoprecipal Antihemophilic Factor Cryoprecipal Antihemophilic Factor AHF Fresh frozen plasma is thawed and contains insoluble components of hemoglobin with suspected fibrinogen and von Willebrand factor (VWF). 7.5 Platelet concentrate 7.5.1 Platelet concentrate Platelet concentrate is prepared from a single portion of whole blood and the platelet count reaches the required level. 7.5 Blood component apheresis 7.6-1 Apheresis The process of extracting one or more components from donated whole blood and returning the remaining components to the donor. 7.6.2 Apheresis f.6.3 Monoclonal plasma: plasma prepared by a single collection machine
7.64 Monoclonal platelets: concentrated platelet suspension prepared by a single collection machine. f.65 Monoclonal granulocytes: granulocytes prepared by a single collection machine. B.1 Labels
81.1 Labels
with text, national symbols, and barcodes 81.2 Blood label or blood callletion bug: a label on the surface of blood produced by the manufacturer that meets the requirements of GB42-13
81.3 Raw blood label3. The number of self-recommended red blood cells should retain at least % of the red blood cell component of the whole blood group and the number of white blood cells should be less than the standard. Sweat: To prevent fever and convulsions, the amount of white blood cell in the product should be less than 11.4 times the amount of 100mg/ml of water. The amount of water should be less than 5X1WST 203291
7.3. 4 Washing red blood cells
remove almost all blood and most of the high red blood cell content of the blood cells 7.3.5 Freezing lamp plastic cells fro2enredbloodcells busy in the ice refining forest, after the high red blood cell content of the washing stone, Shengdao red Yi brittle irrndiatedredbludrells7. 3.6 4
after 250C:y~000Gy radiation dose of red blood cell components: 7.3./Rejuvenated red blood cell purchase rejuvenated The red blood cells that have expired for one day at 2--C are restored to the level of 2.3-phosphoglyceraldehyde 1 (2.3->PG) and triglyceride (ATH) by the method of the left method. 7.4 Plasma components
7.4.1 Fresh frozen plasma treshfranplHsFFF is a single plasma that is stored below -18 within 5 days after blood collection. Note: Alpine plasma is separated within 24 hours after blood collection. Quick-frozen plasma that is not stored below -18 is separated within 24 hours after blood collection. 7.4.3 Frozen plasma, RhP is separated within one week after blood collection and stored below -13°C. 7.4.4 Cryoprecipal Antihemophilic Factor Cryoprecipal Antihemophilic Factor AHF Fresh frozen plasma is thawed and contains insoluble components of hemoglobin with suspected fibrinogen and von Willebrand factor (VWF). 7.5 Platelet concentrate 7.5.1 Platelet concentrate Platelet concentrate is prepared from a single portion of whole blood and the platelet count reaches the required level. 7.5 Blood component apheresis 7.6-1 Apheresis The process of extracting one or more components from donated whole blood and returning the remaining components to the donor. 7.6.2 Apheresis f.6.3 Monoclonal plasma: plasma prepared by a single collection machine
7.64 Monoclonal platelets: concentrated platelet suspension prepared by a single collection machine. f.65 Monoclonal granulocytes: granulocytes prepared by a single collection machine. B.1 Labels
81.1 Labels
with text, national symbols, and barcodes 81.2 Blood label or blood callletion bug: a label on the surface of blood produced by the manufacturer that meets the requirements of GB42-13
81.3 Raw blood label3. The number of self-recommended red blood cells should retain at least % of the red blood cell component of the whole blood group and the number of white blood cells should be less than the standard. Sweat: To prevent fever and convulsions, the amount of white blood cell in the product should be less than 11.4 times the amount of 100mg/ml of water. The amount of water should be less than 5X1WST 203291
7.3. 4 Washing red blood cells
remove almost all blood and most of the high red blood cell content of the blood cells 7.3.5 Freezing lamp plastic cells fro2enredbloodcells busy in the ice refining forest, after the high red blood cell content of the washing stone, Shengdao red Yi brittle irrndiatedredbludrells7. 3.6 4
after 250C:y~000Gy radiation dose of red blood cell components: 7.3./Rejuvenated red blood cell purchase rejuvenated The red blood cells that have expired for one day at 2--C are restored to the level of 2.3-phosphoglyceraldehyde 1 (2.3->PG) and triglyceride (ATH) by the method of the left method. 7.4 Plasma components
7.4.1 Fresh frozen plasma treshfranplHsFFF is a single plasma that is stored below -18 within 5 days after blood collection. Note: Alpine plasma is separated within 24 hours after blood collection. Quick-frozen plasma that is not stored below -18 is separated within 24 hours after blood collection. 7.4.3 Frozen plasma, RhP is separated within one week after blood collection and stored below -13°C. 7.4.4 Cryoprecipal Antihemophilic Factor Cryoprecipal Antihemophilic Factor AHF Fresh frozen plasma is thawed and contains insoluble components of hemoglobin with suspected fibrinogen and von Willebrand factor (VWF). 7.5 Platelet concentrate 7.5.1 Platelet concentrate Platelet concentrate is prepared from a single portion of whole blood and the platelet count reaches the required level. 7.5 Blood component apheresis 7.6-1 Apheresis The process of extracting one or more components from donated whole blood and returning the remaining components to the donor. 7.6.2 Apheresis f.6.3 Monoclonal plasma: plasma prepared by a single collection machine
7.64 Monoclonal platelets: concentrated platelet suspension prepared by a single collection machine. f.65 Monoclonal granulocytes: granulocytes prepared by a single collection machine. B.1 Labels
81.1 Labels
with text, national symbols, and barcodes 81.2 Blood label or blood callletion bug: a label on the surface of blood produced by the manufacturer that meets the requirements of GB42-13
81.3 Raw blood label
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