Fentex 164601FX
Ref 164601FXModel Instrument zum Halten, Zerquetschen und Zerkleinern von Knorpel und Knochen.
Active
CE MDR
Valid until
Not listed
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number42504077052K6 04250407717230 | Date7 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04250407717230 | Date8 Dec 2022 | StatusListed |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Fentex
- Generic Name
- Bone cutting forceps, reusable
- Model / Ref / Catalog
- 164601FX, Instrument zum Halten, Zerquetschen und Zerkleinern von Knorpel und Knochen.
- Description
- Gelfoam Pressure Forceps by House 18 cm, blade 30 x 30 mm
- Primary DI / UDI-DI
- 04250407717230
- Basic UDI-DI
- 42504077052K6
- Direct Marketing DI
- 04250407717230
- FDA Product Code
- LRC
- EMDN Code
- L140502 Ear surgery pliers, reusable
- GMDN Term
- Bone cutting forceps, reusable
- Device Class
- Class I
- Regulation Number
- 874.4420
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from FENTEX medical GmbH
Properties
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