Aesculap
by Aesculap AG Germany EUDAMEDGUDID
Ref FH326R
Product code GDREMDN L010702
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number4039239000001304ZS | Date13 Oct 2025 | StatusActive |
| United States | GUDID listing GUDID | Number04038653165919 | Date22 Apr 2020 | StatusIn distribution |
Coverage
- Active
- Listed
- Not covered
- European Union
- United States
Specification
- Generic Name
- Manual surgical saw, rigid
- Device Name
- Amputation saw
- Model / Ref / Catalog
- FH326R
- Primary DI / UDI-DI
- 04038653165919
- Basic UDI-DI
- 4039239000001304ZS
- Direct Marketing DI
- 04038653165919
- FDA Product Code
- GDR
- EMDN Code
- L010702 Blades for manual surgical saws, reusable
- GMDN Term
- Manual surgical saw, rigid
- Device Class
- Class I
- Regulation Number
- 878.4800
- Market of Registration
- Germany
- Commercial Distribution
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Manufacturer details
- EUDAMED SRN
- DE-MF-000005504
Other devices from Aesculap AG
Properties & raw data
Show properties, registry sources and raw records
Other properties (20)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Expiration Date: No
- Manufacturing Date: No
Sources (2)
- EUDAMED e92a1670-1d88-4f9f-87a9-75b9d8a4c34f
- FDA UDI dc2edc5f-2b97-4dee-a3c0-c1fc57c9aef7