Identity
- Trade Name
- ALPHA EUDAMEDAESCULAP FDA UDI
- Generic Name
- Surgical bulldog clamp, reusable FDA UDI
- Device Name
- Micro Bulldog clip EUDAMEDMUELLER ALPHA Vessel Clip For Arteries, straight, non-traum. (fine cross-serr.), closing force: 0,80 N, micro, non-sterile, reusable FDA UDI
- Model / Reference
- FE020K EUDAMEDFDA UDI
- Description
- MUELLER ALPHA Vessel Clip For Arteries, straight, non-traum. (fine cross-serr.), closing force: 0,80 N, micro, non-sterile, reusable FDA UDI
Identifiers
- Catalog Number
- FE020K FDA UDI
- Primary DI / UDI-DI
- 04038653161195 EUDAMEDFDA UDI
- Basic UDI-DI
- 40392390000019132U EUDAMED
- FDA Product Code
- DXC FDA UDI
- EMDN Code
- L0708010101 BULLDOG VASCULAR CLIPS, REUSABLE EUDAMED
- GMDN Term
- Surgical bulldog clamp, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 870.4450 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
Yes
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
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Alpha by Aesculap AG — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 40392390000019132U | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Aesculap AG
- EUDAMED SRN
- DE-MF-000005504
Sources (2)
- EUDAMED 3837c9b9-d4b1-4e45-8778-4ed85ad5fa44 61 fields · synced Jun 19, 2026
- FDA UDI 8f27d3f6-f76c-4890-9468-13a43762c734 36 fields · synced May 30, 2026