Identity
- Trade Name
- Aesculap EUDAMEDFDA UDI
- Generic Name
- Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI
- Device Name
- ENT forceps Ir EUDAMEDMC GEE Wire Bending Forceps, curved downwards, 3 1/4", (80 mm), (3,50 mm), with tubular shaft FDA UDI
- Model / Reference
- OG359R EUDAMEDFDA UDI
- Description
- MC GEE Wire Bending Forceps, curved downwards, 3 1/4", (80 mm), (3,50 mm), with tubular shaft FDA UDI
Identifiers
- Catalog Number
- OG359R FDA UDI
- Primary DI / UDI-DI
- 04038653051762 EUDAMEDFDA UDI
- Basic UDI-DI
- 4039239000001225ZV EUDAMED
- Direct Marketing DI
- 04038653051762 EUDAMED
- FDA Product Code
- KAE FDA UDI
- EMDN Code
- L140599 EAR SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 874.4420 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
Category: Tuning fork
Aesculap by Aesculap AG — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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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 | 4039239000001225ZV | 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 7b98d0bf-19c1-4b23-b9b7-4f268def7c00 61 fields · synced Jul 8, 2026
- FDA UDI 496fb576-6f5e-4810-b0a6-68253f5d38c3 36 fields · synced May 30, 2026