|
Std ID |
Description (Standard Title) |
Detail |
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YY/T 1205-2013
|
Total bilirubin test kit (Vanadate oxidation method)
|
YY/T 1205-2013
|
|
YY/T 1206-2013
|
Total cholesterol kit (COD-PAP method)
|
YY/T 1206-2013
|
|
YY/T 1213-2013
|
Follicle stimulating hormone quantitative labelling immunoassay kit
|
YY/T 1213-2013
|
|
YY/T 1214-2013
|
Human chorionic gonadotrophin quantitative labelling immunoassay kit
|
YY/T 1214-2013
|
|
YY/T 1216-2013
|
Alpha-fetoprotein quantitative labelling immunoassay kit
|
YY/T 1216-2013
|
|
YY/T 1218-2013
|
Thyroid-stimulating hormone quantitative labelling immunoassay kit
|
YY/T 1218-2013
|
|
YY/T 1231-2014
|
Creatinine test reagent kit (Method of sarcosine oxidase)
|
YY/T 1231-2014
|
|
YY/T 1232-2014
|
Gamma-Glutamyl transpeptadase test reagent kit (Method of GPNA)
|
YY/T 1232-2014
|
|
YY/T 1233-2014
|
Cardiac troponin-I (cTnl) quantitative detection reagent (kit) (Chemiluminescent immunoassay)
|
YY/T 1233-2014
|
|
YY/T 1235-2014
|
Rubella virus IgG / IgM antibody detection kit
|
YY/T 1235-2014
|
|
YY/T 1240-2014
|
D-Dimer reagent (kit)
|
YY/T 1240-2014
|
|
YY/T 1244-2014
|
Purified water for in vitro diagnostic reagents
|
YY/T 1244-2014
|
|
YY/T 1247-2014
|
Hepatitis B virus surface antigen (HBsAg) detection reagent (kit) (chemiluminescent immunoassay)
|
YY/T 1247-2014
|
|
YY/T 1249-2014
|
Free prostate specific antigen quantitative labelling immunoassay kit
|
YY/T 1249-2014
|
|
YY 0308-2004
|
Medical sodium hyaluronate gel
|
YY 0308-2004
|
|
YY 0321.3-2009
|
Single-use filter for anaesthesia
|
YY 0321.3-2009
|
|
YY 0326.1-2002
|
Plasmapheresis centrifuge apparatus for single use - Part 1: Centrifuge bowl
|
YY 0326.1-2002
|
|
YY 0326.2-2002
|
Plasmapheresis centrifuge apparatus for single use - Part 2: Plasma tubing
|
YY 0326.2-2002
|
|
YY 0326.3-2005
|
Plasmapheresis centrifuge apparatus for single use - Part 3: Containers for plasma
|
YY 0326.3-2005
|
|
YY 0341-2009
|
General technological requirements for non-active metallic surgical implants for osteosynthesis
|
YY 0341-2009
|
|
YY 0450.1-2003
|
Accessory devices for sterile single-use intravascular catheters. Part 1: Introducers
|
YY 0450.1-2003
|
|
YY 0285.1-2017
|
Intravascular catheters - Sterile and single-use catheters - Part 1: General requirements
|
YY 0285.1-2017
|
|
YY 0285.3-2017
|
Intravascular catheters—Sterile and single-use catheters—Part 3: Central venous catheters
|
YY 0285.3-2017
|
|
YY 0285.4-2017
|
Intravascular catheters—Sterile and single-use catheters—Part 4: Balloon dilatation catheters
|
YY 0285.4-2017
|
|
YY 0286.3-2017
|
Special infusion sets -- Part 3: Light-resistant infusion sets for single use
|
YY 0286.3-2017
|
|
YY 0762-2017
|
Ophthalmic optical -- Capsular tension ring
|
YY 0762-2017
|
|
YY 0989.7-2017
|
Implants for surgery -- Active implantable medical devices -- Part 7: Particular requirements for cochlear implant systems
|
YY 0989.7-2017
|
|
YY/T 0127.7-2017
|
Biological evaluation of dental materials -- Part 2: Biological evaluation test method of dental materials -- Pulp and dentine usage test
|
YY/T 0127.7-2017
|
|
YY/T 0287-2017
|
Medical devices -- Quality management systems -- Requirements for regulatory purposes
|
YY/T 0287-2017
|
|
YY/T 0326-2017
|
Plasmapheresis centrifuge apparatus for single use
|
YY/T 0326-2017
|
|
YY/T 0471.5-2017
|
Test methods for primary wound dressings—Part 5: Bacterial barrier properties
|
YY/T 0471.5-2017
|
|
YY/T 0490-2017
|
Tracheobronchial tubes—Sizing and marking
|
YY/T 0490-2017
|
|
YY/T 0492-2017
|
Implantable cardiac pacing lead
|
YY/T 0492-2017
|
|
YY/T 0614-2017
|
Single-use high-pressure angiographic syringes and accessories
|
YY/T 0614-2017
|
|
YY/T 0618-2017
|
Test methods for bacterial endotoxins of medical devices—Routine monitoring and alternatives to batch testing
|
YY/T 0618-2017
|
|
YY/T 0619-2017
|
Medical endoscopes--Rigid resectosocope
|
YY/T 0619-2017
|
|
YY/T 0653-2017
|
Hematology analyzer
|
YY/T 0653-2017
|
|
YY/T 0654-2017
|
Automatic chemistry analyzer
|
YY/T 0654-2017
|
|
YY/T 0657-2017
|
Medical centrifuge
|
YY/T 0657-2017
|
|
YY/T 0659-2017
|
Blood coagulation analyzer
|
YY/T 0659-2017
|
|
YY/T 0686-2017
|
Medical forceps
|
YY/T 0686-2017
|
|
YY/T 0706-2017
|
Particular specifications for mammographic X-ray equipment
|
YY/T 0706-2017
|
|
YY/T 1122-2017
|
General technique requirememts for orthopaedics clamp(scissor)
|
YY/T 1122-2017
|
|
YY/T 1137-2017
|
General technique requirements for orthopaedics saw
|
YY/T 1137-2017
|
|
YY/T 1292.4-2017
|
Test for reproductive and developmental toxicity of medical devices—Part 4: Two-generation reproductive toxicity test
|
YY/T 1292.4-2017
|
|
YY/T 1293.5-2017
|
Contacting wound dressing—Part 5: Alginate dressing
|
YY/T 1293.5-2017
|
|
YY/T 1403-2017
|
Requirements of contract sterilization using ethylene oxide
|
YY/T 1403-2017
|
|
YY/T 1465.4-2017
|
Immunogenic evaluation method of medical devices—Part 4: Phagocytosis of mouse peritoneal macrophages on chicken erythrocytes—Ex-vivo method
|
YY/T 1465.4-2017
|
|
YY/T 1477.4-2017
|
Standard test models for primary wound dressing performance evaluation—Part 4: In vitro wound model for adhesion properties evaluation of dressings
|
YY/T 1477.4-2017
|
|
YY/T 1510-2017
|
Medical plasma virus inactivated device
|
YY/T 1510-2017
|
|
YY/T 1511-2017
|
Collagen sponge
|
YY/T 1511-2017
|
|
YY/T 1512-2017
|
Biological evaluation of medical devices—Guidance on the conduct of biological evaluation within a risk management process
|
YY/T 1512-2017
|
|
YY/T 1513-2017
|
C-reactive protein testing kit
|
YY/T 1513-2017
|
|
YY/T 1514-2017
|
Detection kit for antibodies to HIV-1 and HIV-2(western blotting)
|
YY/T 1514-2017
|
|
YY/T 1515-2017
|
HIV-1 RNA quantitative assay
|
YY/T 1515-2017
|
|
YY/T 1516-2017
|
Prolactin quantitative labelling immunoassay kit
|
YY/T 1516-2017
|
|
YY/T 1517-2017
|
Detection kit for IgA antibody to epstein-barr viral capsid antigens
|
YY/T 1517-2017
|
|
YY/T 1518-2017
|
C-peptide quantitative labelling immunoassay kit
|
YY/T 1518-2017
|
|
YY/T 1519-2017
|
Electrophysiology catheter
|
YY/T 1519-2017
|
|
YY/T 1521-2017
|
Technical requirements for sonoelasticity tissue-mimicking phantom
|
YY/T 1521-2017
|
|
YY/T 1522-2017
|
Flow-metering devices for connection to terminal units of medical gas pipeline systems
|
YY/T 1522-2017
|
|
YY/T 1523-2017
|
Bicarbonate assay kit(PEPC enzymatic method)
|
YY/T 1523-2017
|
|
YY/T 1524-2017
|
α-L-Fucosidase(AFU) assay kit(CNPF substrate method)
|
YY/T 1524-2017
|
|
YY/T 1525-2017
|
Test kit for methamphetamine (colloidal gold method)
|
YY/T 1525-2017
|
|
YY/T 1526-2017
|
Detection kit for human immunodeficiency virus 1 type(HIV-1) p24 antigen and antibodies to human immunodeficiency virus(chemiluminescence immuno-assay)
|
YY/T 1526-2017
|
|
YY/T 1527-2017
|
α/β-Thalassemia gene typing detection kit
|
YY/T 1527-2017
|
|
YY/T 1528-2017
|
Myoglobin assay kit(immunoturbidimetric method)
|
YY/T 1528-2017
|
|
YY/T 1529-2017
|
ELISA analytical instruments
|
YY/T 1529-2017
|
|
YY/T 1530-2017
|
Control materials for urine formed element analyzer
|
YY/T 1530-2017
|
|
YY/T 1531-2017
|
Biochemical identification systems for bacteria
|
YY/T 1531-2017
|
|
YY/T 1532-2017
|
Biological evaluation of medical devices—Nanomaterials—Hemolysis test
|
YY/T 1532-2017
|
|
YY/T 1533-2017
|
Automatic time-resolved fluorescence counter
|
YY/T 1533-2017
|
|
YY/T 1534-2017
|
Measuring methods for optical radiation safety classification of medical LED equipment
|
YY/T 1534-2017
|
|
YY/T 1535-2017
|
Medical devices for human in vitro assisted reproductive technology—Biological evaluation—Human sperm survival assay
|
YY/T 1535-2017
|
|
YY/T 1536-2017
|
Catheters other than intravascular catheters—Standard test model for evaluating the surface sliding performance
|
YY/T 1536-2017
|
|
YY/T 1537-2017
|
Laser positioning system in radiation therapy—Functional-performance characteristics and test methods
|
YY/T 1537-2017
|
|
YY/T 1538-2017
|
Auto-scanning water phantom system in radiation therapy—Functional-performance characteristics and test methods
|
YY/T 1538-2017
|
|
YY/T 1539-2017
|
Medical clean bench
|
YY/T 1539-2017
|
|
YY/T 1540-2017
|
Guide for the check of medical class Ⅱ biological safety cabinets
|
YY/T 1540-2017
|
|
YY/T 1541-2017
|
Specification for high voltage cable assemblies and sockets of Mammographic X-ray equipment
|
YY/T 1541-2017
|
|
YY/T 1542-2017
|
Evaluation method of automatic exposure control in digital medical X-ray equipment
|
YY/T 1542-2017
|
|
YY/T 1543-2017
|
Nasal oxygen cannula
|
YY/T 1543-2017
|
|
YY/T 1544-2017
|
Ethylene oxide sterilization safety and effectiveness basic supply requirements
|
YY/T 1544-2017
|
|
YY/T 1545-2017
|
Evaluation of connection between haemodialysis concentrate and haemodialysis equipment
|
YY/T 1545-2017
|
|
YY/T 1546-2017
|
Testing method for SPECT imaging based on CT-attenuation correction
|
YY/T 1546-2017
|
|
YY/T 1547.1-2017
|
Immobilization device for body positioning used in radiation therapy—Part 1: Thermoplastic
|
YY/T 1547.1-2017
|
|
YY/T 1547.2-2017
|
Immobilization device for body positioning used in radiation therapy—Part 2: Vacuum cushion
|
YY/T 1547.2-2017
|
|
YY/T 1548-2017
|
Film dose measurement methods used in radiation therapy
|
YY/T 1548-2017
|
|
YY/T 1549-2017
|
Calibrator for Biochemical Analyzer
|
YY/T 1549-2017
|
|
YY/T 1550.1-2017
|
Guidance of study on the compatibility of infusion equipments and pharmaceutical products—Part 1: Drug sorption
|
YY/T 1550.1-2017
|
|
YY/T 1551.1-2017
|
Air filters for medical infusion and transfusion equipments—Part 1: Aerosol bacterial retention test method
|
YY/T 1551.1-2017
|
|
YY/T 1551.2-2017
|
Air filters for medical infusion and transfusion equipments—Part 2: Liquid bacterial retention test method
|
YY/T 1551.2-2017
|
|
YY/T 1551.3-2017
|
Air filters for medical infusion and transfusion equipments—Part 3: Integrity test methods
|
YY/T 1551.3-2017
|
|
YY/T 1554-2017
|
Oviduct catheter
|
YY/T 1554-2017
|
|
YY/T 1555.1-2017
|
Particular requirement of silicone gel filled breast implant—Performance requirement of silicone gel filler—Part 1: Limitation requirement of volatile substances
|
YY/T 1555.1-2017
|
|
YY/T 1556-2017
|
Test methods for particle contamination of infusion, transfusion and injection equipments for medical use
|
YY/T 1556-2017
|
|
YY/T 1557-2017
|
Thermoplastic polyurethane(TPU) materials for manufacture of infusion, transfusion and injection equipments for medical use
|
YY/T 1557-2017
|
|
YY/T 1559-2017
|
Spinal implants—Standard test methods for static and dynamic characterization of spinal artificial discs
|
YY/T 1559-2017
|
|
YY/T 1560-2017
|
Spinal implant—Standard test methods for occipital-cervical and occipital-cervical-thoracic implant constructs in a vertebrectomy model
|
YY/T 1560-2017
|
|
YY/T 1561-2017
|
Tissue engineering medical device products - Remnant α-Gal antigen determination in scaffold materials utilizing animal tissues and their derivatives
|
YY/T 1561-2017
|