Aesculap
by Aesculap AG Germany EUDAMEDGUDID
Ref FK507R
Product code HTPEMDN L091202
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number403923900000130825 | Date18 Nov 2025 | StatusActive |
| United States | GUDID listing GUDID | Number04038653166534 | Date22 Apr 2020 | StatusIn distribution |
Coverage
- Active
- Listed
- Not covered
- European Union
- United States
Specification
- Generic Name
- Bone file/rasp, manual, reusable
- Device Name
- Bone file/rasp
- Model / Ref / Catalog
- FK507R
- Primary DI / UDI-DI
- 04038653166534
- Basic UDI-DI
- 403923900000130825
- Direct Marketing DI
- 04038653166534
- FDA Product Code
- HTP
- EMDN Code
- L091202 Orthopaedic surgery files, reusable
- GMDN Term
- Bone file/rasp, manual, reusable
- Device Class
- Class I
- Regulation Number
- 888.4540
- 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 8a813da8-f2b2-44ef-8285-659c8f7510b4
- FDA UDI 06a6d3cd-70f4-4178-ba14-43476fc9b170