Identity
- Trade Name
- Aesculap EUDAMEDFDA UDI
- Generic Name
- Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI
- Device Name
- Grasping forceps EUDAMEDSpermatic Cord Fixation Clamp, 5 3/4", (145 mm), non-sterile, reusable FDA UDI
- Model / Reference
- EF195R EUDAMEDFDA UDI
- Description
- Spermatic Cord Fixation Clamp, 5 3/4", (145 mm), non-sterile, reusable FDA UDI
Identifiers
- Catalog Number
- EF195R FDA UDI
- Primary DI / UDI-DI
- 04038653151806 EUDAMEDFDA UDI
- Basic UDI-DI
- 40392390000004712A EUDAMED
- Direct Marketing DI
- 04038653151806 EUDAMED
- FDA Product Code
- HXD FDA UDI
- EMDN Code
- L03130401 TISSUE AND ORGAN GRASPING FORCEPS, REUSABLE EUDAMED
- GMDN Term
- Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 878.4800 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
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
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
Yes
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
Aesculap 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 | 40392390000004712A | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Aesculap AG
- EUDAMED SRN
- DE-MF-000005504
Sources (2)
- EUDAMED 77b30106-1a29-46a7-b0fe-7a3d0a176cde 61 fields · synced May 30, 2026
- FDA UDI bd502a84-0a69-4cf9-8730-b9236cb25a67 35 fields · synced May 30, 2026