Anthogyr ACCESSOIRIES
FDA UDIEUDAMEDClass I (US FDA UDI)
Identity
- Trade Name
- Anthogyr ACCESSOIRIES FDA UDI
- Generic Name
- Device sterilization/disinfection container, reusable FDA UDI
- Model / Reference
- 5932S EUDAMEDFDA UDISterilization box EUDAMED
Identifiers
- Catalog Number
- 5932S FDA UDI
- Primary DI / UDI-DI
- 03663394483353 EUDAMEDFDA UDI
- Basic UDI-DI
- 36633940073R5 EUDAMED
- FDA Product Code
- EIS FDA UDI
- EMDN Code
- V0599 CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
- GMDN Term
- Device sterilization/disinfection container, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 872.4565 FDA UDI
- Market of Registration
- France EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
No
Implantable
No
Reusable
No
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
No
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
Yes
Category: Device sterilization/disinfection container, reusable
Anthogyr ACCESSOIRIES by Etablissements Anthogyr — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Etablissements Anthogyr
Sources (2)
- FDA UDI 9f4b0d31-d80e-41b6-8f62-fd9d613618b9 33 fields · synced Jun 20, 2026
- EUDAMED 1483fd98-b91d-48d7-883a-c43cb63d10e9 61 fields · synced Jun 20, 2026