Identity
- Device Name
- Trial shell size 42 EUDAMED
- Model / Reference
- 800032 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07640164281704 EUDAMED
- Basic UDI-DI
- B-07640164281704 EUDAMED
- EMDN Code
- L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Trial shell size 42 by Atesos medical AG — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-07640164281704 | Class I | Active |
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Manufacturer
- Manufacturer
- Atesos medical AG
- EUDAMED SRN
- CH-MF-000010304
- Authorised Representative
- hestomed GmbH DE-AR-000006853
Sources (1)
- EUDAMED dc48acf6-487c-41d6-a603-566677b4f61a 61 fields · synced Jul 24, 2026