Identity
- Trade Name
- Aesculap EUDAMEDFDA UDI
- Generic Name
- Self-retaining surgical retractor, reusable FDA UDI
- Device Name
- Abdominal/bladder/liver retractor IIa EUDAMEDGOSSET Abdominal Retractor, complete retractor, small, blades 38 mm deep, depth: 125 mm, width: 115 mm, opening width: 110 mm, non-sterile, reusable FDA UDI
- Model / Reference
- BV500R EUDAMEDFDA UDI
- Description
- GOSSET Abdominal Retractor, complete retractor, small, blades 38 mm deep, depth: 125 mm, width: 115 mm, opening width: 110 mm, non-sterile, reusable FDA UDI
Identifiers
- Catalog Number
- BV500R FDA UDI
- Primary DI / UDI-DI
- 04038653032280 EUDAMEDFDA UDI
- Basic UDI-DI
- 40392390000024832X EUDAMED
- Direct Marketing DI
- 04038653032280 EUDAMED
- FDA Product Code
- FFO FDA UDI
- EMDN Code
- L040901 ABDOMINAL SPREADERS, REUSABLE EUDAMED
- GMDN Term
- Self-retaining surgical retractor, reusable FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 876.4730 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
No
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 IIa — 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 | 40392390000024832X | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | 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 b9094aac-cbd3-430b-8de0-f3e3e926a79e 61 fields · synced May 30, 2026
- FDA UDI 73c536d4-bd24-4a72-9efd-c378783b17b9 35 fields · synced May 30, 2026