Identity
- Device Name
- Set soin EUDAMED
- Model / Reference
- 4801236 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07640178433212 EUDAMED
- Basic UDI-DI
- B-07640178433212 EUDAMED
- EMDN Code
- V9012 NON-SPECIALIST SURGICAL INSTRUMENTS AND KITS, SINGLE-USE EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Romania EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
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
Category: Surgical retractor/retraction system blade, single-use
Set soin by Applimed SA — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS
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Also classified as Surgical retractor/retraction system blade, single-use.
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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-07640178433212 | Class I | Active |
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Manufacturer
- Manufacturer
- Applimed SA
- EUDAMED SRN
- CH-MF-000046641
- Authorised Representative
- Dansu A/S DK-AR-000046254
Sources (1)
- EUDAMED a7e6d47b-e589-46f9-bd27-62a4356c66d4 61 fields · synced Jun 19, 2026