Identity
- Trade Name
- Aesculap EUDAMEDFDA UDI
- Generic Name
- Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI
- Device Name
- Tissue grasping forceps EUDAMEDKRAEMER Grasping Forceps, straight, 6", (150 mm), working length: 4 3/4", (120 mm), toothed (1x2), with ratchet, width: 3 mm FDA UDI
- Model / Reference
- FO820R EUDAMEDFDA UDI
- Description
- KRAEMER Grasping Forceps, straight, 6", (150 mm), working length: 4 3/4", (120 mm), toothed (1x2), with ratchet, width: 3 mm FDA UDI
Identifiers
- Catalog Number
- FO820R FDA UDI
- Primary DI / UDI-DI
- 04038653169443 EUDAMEDFDA UDI
- Basic UDI-DI
- 40392390000006552N EUDAMED
- Direct Marketing DI
- 04038653169443 EUDAMED
- FDA Product Code
- HTD FDA UDI
- EMDN Code
- L110602 NEUROSURGERY GRIPPERS, 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
Category: Flexible endoscopic biopsy forceps, reusable
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 | 40392390000006552N | 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 2e9f04bf-7553-43c0-bea3-8911c206be82 61 fields · synced May 30, 2026
- FDA UDI 9e3bad2f-a5be-4fcc-a625-2da23f00adfa 36 fields · synced May 30, 2026