Identity
- Trade Name
- Aesculap EUDAMED
- Device Name
- Standard Wound Retractor Ir EUDAMED
- Model / Reference
- BT178R EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04038653141043 EUDAMED
- Basic UDI-DI
- 403923900000117428 EUDAMED
- Direct Marketing DI
- 04038653141043 EUDAMED
- EMDN Code
- L03140104 SPREADERS HOOKS, REUSABLE 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
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Aesculap by Aesculap AG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 403923900000117428 | Class I | Active |
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Manufacturer
- Manufacturer
- Aesculap AG
- EUDAMED SRN
- DE-MF-000005504
Sources (1)
- EUDAMED b816bbd4-f429-441f-b052-609c97ea5702 61 fields · synced May 23, 2026