YY/T 0308-2015 PDF English
US$150.00 · In stock · Download in 9 secondsYY/T 0308-2015: Medical sodium hyaluronate gel Delivery: 9 seconds. True-PDF full-copy in English & invoice will be downloaded + auto-delivered via email. See step-by-step procedureStatus: Valid YY/T 0308: Evolution and historical versions
Standard ID | Contents [version] | USD | STEP2 | [PDF] delivery | Name of Chinese Standard | Status |
YY/T 0308-2015 | English | 150 |
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Medical sodium hyaluronate gel
| Valid |
YY 0308-2004 | English | 160 |
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Medical sodium hyaluronate gel
| Obsolete |
YY 0308-1998 | English | 399 |
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Medical hyaluronan gel
| Obsolete |
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YY/T 0308-2015: Medical sodium hyaluronate gel---This is an excerpt. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.), auto-downloaded/delivered in 9 seconds, can be purchased online: https://www.ChineseStandard.net/PDF.aspx/YYT0308-2015
YY
PHARMACEUTICAL INDUSTRY STANDARD
ICS 11.120.20
C 48
Replacing YY/T 0308-2004
Medical sodium hyaluronate gel
Issued on. MARCH 2, 2015
Implemented on. JANUARY 1, 2016
Issued by. China Food and Drug Administration
Table of Contents
Foreword... 3
Introduction... 5
1 Scope... 7
2 Normative references... 7
3 Terms and definitions... 7
4 Classification... 8
5 Requirements... 8
6 Inspection rules... 12
7 Marks... 12
8 Packaging... 13
Appendix A... 14
Appendix B... 17
Appendix C... 19
Appendix D... 21
References... 23
Foreword
This Standard was drafted in accordance with the rules given in GB/T 1.1-2009.
This Standard replaces YY 0308-2004 Medical sodium hyaluronate gel.
Compared with YY 0308-2004, the main technical changes are as follows.
- Added terms, definitions and requirements for shear viscosity, elasticity,
viscoelastic and weight average molecular weight (see 3.2~3.5, 5.8, 5.9,
5.10.2 of this edition);
- Deleted dynamic viscosity’s terms, definitions and requirements (3.2 of this
edition; 5.8 of 2004 edition);
- Modified requirements for effective usage (see 5.2 of this edition; 5.2 of
2004 edition);
- Modified requirements for light transmittance (see 5.5 of this edition; 5.5 of
2004 edition);
- Modified requirements for protein content (5.11 of this edition; 5.10 of 2004
edition);
- Added requirements for refractive index (see 5.13 of this edition);
- Modified ethanol residues indicator (see 5.15 of this edition; 5.13 of 2004
edition);
- Modified bacterial endotoxin Indicator (see 5.17 of this edition; 5.15 of 2004
edition);
- Deleted description on biological test methods (5.17.2~5.17.7 of 2004
edition);
- Modified method for the determination of sodium hyaluronate (see
Appendix A of this edition; Appendix A of 2004 edition).
Please note that some of the content of this document may involve patents; the
issuing agency of this document does not undertake the responsibility for the
identification of these patents.
This Standard was proposed by China Food and Drug Administration.
This Standard shall be under the jurisdiction of Shandong Food and Drug
Administration of China Food and Drug Administration.
The drafting organizations of this Standard. Shanghai Qisheng Biological
Agents Ltd., Shandong Quality Inspection Center for Medical Devices, and
Shandong Freda Biotechnology Co., Ltd.
Main drafters of this Standard. Wang Wenbin, Jiang Lixia, Shen Yong, Liu Lili,
Liu Ye, Guo Xueping, and Mu Shue.
This Standard was issued in October, 1998 for the first time, and amended in
November, 2004.This edition is the second revision.
1 Scope
This Standard specifies the classification, requirements, inspection rules, marks
and packaging of medical sodium hyaluronate gel.
This Standard is applicable to medical sodium hyaluronate gel. The application
of medical sodium hyaluronate gel includes viscoelastic agents for eye surgery,
lubricants for intra-articular injection and barriers for surgical operation.
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 (including any
amendments) applies.
GB/T 16886.1 Biological evaluation of medical devices - Part 1.Evaluation
and testing within a risk management process
Pharmacopoeia of the People's Republic of China 2010 English Edition, 2
Volumes
3 Terms and definitions
The following terms and definitions apply to this document.
3.1 medical sodium hyaluronate gel
Gel-like solution formulated with sodium hyaluronate and for human.
3.2 shear viscosity
Ability to resist deformation rate of fluid by shear force.
3.3 elasticity
After the material is deformed by an external force, the external force is
removed to restore nature to its original shape.
4 Classification
4.1 Medical sodium hyaluronate gel is divided by clinical applicability into. for
ophthalmic use, for surgical use and for intra-articular injection use.
4.2 Medical sodium hyaluronate gel is generally divided according to product
packaging specifications into.
5 Requirements
5.1 Appearance
According to Appendix IX H of Pharmacopoeia of the People's Republic of
China 2010 English Edition, 2 Volumes,
5.2 Effective usage
Try to take out the content in each single package in normal used method. After
accurately weighed, it is divided by medical sodium hyaluronate gel density (ρ
= 1.01 g/mL), the obtained value shall not be less than 93% of the labelled
amount, and the average value shall not be less than the labelled amount.
5.3 Identification
Medical sodium hyaluronate gel shall have the following reactions.
5.4 Content
Determine it according to the method stipulated in Appendix A and the sodium
hyaluronate content should be 90.0%~120.0% of the labelled mass
concentration.
5.5 Light transmittance
Use sodium chloride solution of which the concentration is 9 g/L for 10-fold
dilution of medical sodium hyaluronate gel. Take preparation solution as blank
control.
5.6 pH
Use distilled water for equivalent mass ration dilution of medical sodium
hyaluronate gel. Determine pH according to the method stipulated in Appendix
VI H of Pharmacopoeia of the People's Republic of China 2010 English Edition,
2 Volumes, and pH shall be within 6.8~7.6.
5.9 Elasticity
For sodium hyaluronate used for ophthalmology and intra-articular, it shall use
rheometer to conduct frequency scan at shear rate of 0.01 Hz ~ 100 Hz at
(25±0.2)°C. Draw logarithmic line graphs of viscous modulus G" and elastic
modulus G' and logarithmic line graph of frequency. The shear frequency
corresponding to G" = G' shall be less than the labelled value.
5.10 The average molecular weight
5.10.2 Weight average molecular weight and molecular weight
distribution factor
5.11 Protein content
Determine in the method stipulated in Appendix C. The protein content in
sodium hyaluronate shall not be greater than 0.1% (mass fraction).
5.15 The residual amount of ethanol
Determine in the method stipulated in Appendix D. The residual amount of
ethanol in medical sodium hyaluronate gel shall not be greater than 200 µg/g.
5.16 Sterility
Inspect in the method stipulated in Appendix XI H of the People's Republic of
China 2010 English Edition, 2 Volumes. Medical sodium hyaluronate gel should
be sterile.
5.17 Bacterial endotoxin
Use bacterial endotoxin test water to dilute the medical sodium hyaluronate gel.
Inspect by the method stipulated in Appendix XI E of the People's Republic of
China 2010 English Edition, 2 Volumes. Bacterial endotoxin per milliliter of
medical sodium hyaluronate gel shall be less than 0.5 EU.
6 Inspection rules
6.1 Group-batch
Medical sodium hyaluronate gel feed of same batch shall be produced in same
feeling and same technology.
6.2 Type inspection
7 Marks
7.1 The following marks shall be on the bulk packaging.
7.2 The following marks shall be on the small packaging or accompanying
documentation.
8 Packaging
It shall use a dose packaging for the small packaging of medical sodium
hyaluronate gel shall use. Packaging design of convenient use is preferred.
...... Source: Above contents are excerpted from the full-copy PDF -- translated/reviewed by: www.ChineseStandard.net / Wayne Zheng et al.
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