UNI EN ISO 24998 : 2009
Current
The latest, up-to-date edition.
PLASTICS LABORATORY WARE - SINGLE-USE PETRI DISHES FOR MICROBIOLOGICAL PROCEDURES
19-03-2009
Foreword
1 Scope
2 Terms and definitions
3 Principle of use
4 Types
5 Material
6 Design and construction
6.1 General
6.2 Dimensions
6.3 Rim on lid
6.4 Compartments
6.5 Venting
7 Performance
7.1 Rigidity
7.2 Resistance to thermal distortion
7.3 Resistance to fracture
7.4 Stability in stacking
8 Limitation of contamination
9 Sterility and special microbiological states
10 Packaging
11 Marking
Annex A (normative) - Type test for rigidity
Annex B (normative) - Type test for resistance to
thermal distortion
Annex C (normative) - Type test for resistance to
fracture
Annex D (normative) - Type test for stability in
stacking
Bibliography
Describes requirements and test methods for plain, single-use Petri dishes for microbiological use.
| DocumentType |
Test Method
|
| PublisherName |
Ente Nazionale Italiano di Unificazione (UNI)
|
| Status |
Current
|
| Standards | Relationship |
| ISO 24998:2008 | Identical |
| EN ISO 24998:2008 | Identical |
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| ISO 14644-8:2013 | Cleanrooms and associated controlled environments Part 8: Classification of air cleanliness by chemical concentration (ACC) |
| ISO 14644-2:2015 | Cleanrooms and associated controlled environments Part 2: Monitoring to provide evidence of cleanroom performance related to air cleanliness by particle concentration |
| ISO 14644-5:2004 | Cleanrooms and associated controlled environments — Part 5: Operations |
| ISO 14644-3:2005 | Cleanrooms and associated controlled environments Part 3: Test methods |
| ISO 14644-7:2004 | Cleanrooms and associated controlled environments — Part 7: Separative devices (clean air hoods, gloveboxes, isolators and mini-environments) |
| ISO 14644-1:2015 | Cleanrooms and associated controlled environments Part 1: Classification of air cleanliness by particle concentration |
| ISO 14644-4:2001 | Cleanrooms and associated controlled environments — Part 4: Design, construction and start-up |
| ISO 17665-1:2006 | Sterilization of health care products — Moist heat — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices |
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