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relavant therapics -haemodialysers biological evaluation biological evaluation chemical analysis methods gb/t biological evaluation medical devices salt spray proofing coating painting process carbon fluoride 3804-2004 standard
YY 0053-2016 in English

YY 0053-2016 in English

VALID

Hemodialysis and relavant therapics -Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators

  • Issued on:2016-03-23
  • Implemented on:2018-01-01
  • File Format:PDF
  • Delivery:Via email within 1~3 business days
Price(USD): $110.00
$107.00
Standard No: YY 0053-2016
Document status: VALID
Title in English: Hemodialysis and relavant therapics -Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
Title in Chinese: 血液透析及相关治疗血液透析器、血液透析滤过器、血液滤过器和血液浓缩器
Language: English
File Format: Electronic (PDF)
Delivery: Via email within 1~3 business days
Issued on: 2016-03-23
Implemented on: 2018-01-01
Superseding: YY 0053-2008 Cardiovascular implants and artificial organs—Haemodialysers haemodiafilters haemofilters and haemoconcentrators
ICS Classification: 11.040.30-Surgical instruments and materials
Chinese Classification: C45-Extracorporeal circulation, artificial organ and prosthesis device
Professional Classification: YY-Pharmaceutics
Related Keywords: relavant therapics -haemodialysers
biological evaluation biological evaluation
chemical analysis methods gb/t
biological evaluation
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1 Scope

This Standard specifies technical requirements for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators, hereinafter collectively referred to as “the device”, for use in humans.
This Standard is not applicable to:
- extracorporeal blood circuits;
- plasmafilters;
- haemoperfusion devices;
- vascular access devices;
- blood pump;
- pressure monitors for the extracorporeal blood circuit;
- air detection devices;
- systems to prepare, maintain or monitor dialysis fluid;
- systems used to perform therapy of haemodialysis, haemofiltration or haemodiafiltration;
- reprocessing procedures and equipment.
Note: Requirements for the extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters are specified in YY 0267-2016.

2 Normative References

The following referenced documents are indispensable for the application of this Document. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (include any amendments) applies.
GB/T 1962.2 Conical Fittings with a 6% (Luer) Taper For Syringes, Needles and Certain Other Medical Equipment - Part 2: Lock Fittings(GB/T 1962.2-2001, ISO 594-2:1998,IDT)
GB/T 14233.1-2008 Test Methods for Infusion, Transfusion, Injection Equipment for Medical Use - Part 1: Chemical Analysis Methods
GB/T 16886.1 Biological Evaluation of Medical Devices - Part 1: Evaluation and Testing within a Risk Management Process(GB/T 16886.1-2011; ISO 10993-1:2009, IDT)
Pharmacopoeia of People's Republic of China, Edition 2010

3 Requirements

3.1 Biological evaluation
Biological evaluation on hazard of part directly or indirectly contacted to blood in product shall be conducted.
3.2 Sterility
The product shall be free from any bacterium after the confirmed sterilization process.
3.3 Non-pyrogeneity
The product shall be free from pyrogenicity.
3.4 Mechanical characteristics

Foreword I
1 Scope
2 Normative References
3 Requirements
4 Test Methods
5 Labelling
Appendix A (Informative) Technical Differences between this Standard and ISO 8637: 2010 and their Reasons
References

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