Aesculap
by Aesculap AG Germany EUDAMEDGUDID
Ref FK173R
Product code GEGEMDN L0902
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number40392390000003692J | Date16 Sep 2025 | StatusActive |
| United States | GUDID listing GUDID | Number04038653045105 | Date20 Apr 2020 | StatusIn distribution |
Coverage
- Active
- Listed
- Not covered
- European Union
- United States
Specification
- Generic Name
- Open-surgery dissector
- Model / Ref / Catalog
- FK173R
- Primary DI / UDI-DI
- 04038653045105
- Basic UDI-DI
- 40392390000003692J
- Direct Marketing DI
- 04038653045105
- FDA Product Code
- GEG
- EMDN Code
- L0902 Orthopaedic surgery levers, reusable
- GMDN Term
- Open-surgery dissector
- 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 f08e5e0b-bb0c-4f5c-b08a-6cf649121967
- FDA UDI 0d880707-726c-48c2-9111-1de85d6b0009