Identity
- Trade Name
- ATRAUMATA® EUDAMEDATRAUMATA FDA UDI
- Generic Name
- Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI
- Device Name
- Grasping forceps EUDAMEDBABCOCK ATRAUMATA Organ And Tisue Grasping Force, straight, 9 1/2", (240 mm), toothing DE BAKEY, non-sterile, reusable FDA UDI
- Model / Reference
- MD470 EUDAMEDFDA UDI
- Description
- BABCOCK ATRAUMATA Organ And Tisue Grasping Force, straight, 9 1/2", (240 mm), toothing DE BAKEY, non-sterile, reusable FDA UDI
Identifiers
- Catalog Number
- MD470 FDA UDI
- Primary DI / UDI-DI
- 04046963365530 EUDAMEDFDA UDI
- Basic UDI-DI
- 40392390000004712A EUDAMED
- Direct Marketing DI
- 04046963365530 EUDAMED
- FDA Product Code
- HTD FDA UDI
- EMDN Code
- L08050201 PULMONARY TISSUE 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
Atraumata® 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Aesculap AG
- EUDAMED SRN
- DE-MF-000005504
Sources (2)
- EUDAMED 362d3b8e-3ee3-4777-97d0-c6bde1cb1baa 61 fields · synced Jun 18, 2026
- FDA UDI 82dafcee-6f60-4c38-8667-c2f9afdcd600 35 fields · synced May 30, 2026