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YY 0713-2009Dental gypsum-bonded casting investments (English PDF)

牙科石膏结合剂铸造包埋材料

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Issued by

NMPA

Level / Type

Industry · Mandatory

Issue date

June 16, 2009

Implementation date

December 1, 2010

Scope

YY 0713-2009 is the English-translated version of 牙科石膏结合剂铸造包埋材料.

YY 0713-2009 is the Chinese pharmaceutical industry standard for the dental gypsum-bonded casting investment.

It classifies these investments and sets the performance requirements for each class together with the test methods that decide compliance, covering the setting time and the consistency, the setting and thermal expansion, the compressive strength and the detail reproduction, and the information supplied with the material. Issued on 16 June 2009, it has applied since 1 December 2010.

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Document preview — YY 0713-2009

National Standard of the People's Republic of China

ICS
11.060.10
Classification
C 33

Issued by: National Medical Products Administration of the People's Republic of China

Contents

  • Foreword
  • 1 Scope
  • 2 Terms and definitions
  • 4 Requirements
  • 5 Sampling, test environment and reconcile

Foreword

All technical contents of this standard is mandatory.

This standard is identical with ISO 7490:2000 "Dental gypsum bonded casting investment material." This standard is based on ISO 7490:2000 re-drafted.

Original International Standard ISO 1562:1993 has been ISO 22674:2006 replaced so in this standard references were modify.

1 Scope

This standard specifies the classification and performance requirements of dental gypsum bonded casting investment material and the corresponding test methods.

2 Terms and definitions

The following terms and definitions apply to this standard.

2.1 Gypsum-bonded investment powder

A powder mixture consisting of silica and calcium sulfate hemihydrate and/or other refractory component.

NOTE: powders may include small amounts of modifier.

Category 3 Combined with dental plaster casting investments are classified as follows.

--- Type 1; for inlays and crowns.

--- Type 2. for full and partial denture base port.

Some of the material is not limited to this category of one type.

4 Requirements

4.1 Appearance powder

Liquidity 4.2 hours when By 6.2 test, the cured material is at least the diameter of type 1 60mm, Type 2 at least 40mm.

4.3 Clotting time

Press the test measured 6.3 clotting time and coagulation time manufacturers should provide no greater than 20%. If the manufacturer provide for A time range, the coagulation time should the value of the intermediate time range no greater than 20%.

4.4 Compressive strength Press

Test 6.4, the compressive strength of the material of a minimum type of 2.3MPa, type 2 minimum 2.6MPa.

4.6 Linear thermal expansion coefficient

By 6.6 test, linear coefficient of thermal expansion material manufacturer should provide a value no greater than 20%. If the manufacturer provide for a range of values Wai, the measured value should be in the middle of the range of values differ by not more than 20%.

5 Sampling, test environment and reconcile

5.1 Sampling

Take the same batch sufficient retail packing material at least 5kg. In addition to sealing the packaging material should not give up.

If Bulk powder is then mixed thoroughly before testing and should be stored in a moisture-proof container.

6.1 Appearance of the powder

Test by naked eye observation, the powder should be uniform, no lumps and foreign matter.

6.5 Setting expansion

Test Press, curable plant expansion should provide a value no greater than 20%. If the manufacturer provide for a range of values, The measured value should be in the middle of the range of values differ by not more than 20%.

......
This preview omits tables, figures, formulas and parts of the technical clauses. The complete document — 21 pages — is available in the English PDF.

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