Hu-Friedy
by Hu-Friedy Manufacturing Co., LLC United States EUDAMEDGUDID
Ref F23ISModel Dental Device
Product code EMGEMDN L150301
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number0889950Hinged1RQN | Date27 May 2025 | StatusActive |
| United States | GUDID listing GUDID | Number10889950113001 | Date22 Feb 2023 | StatusIn distribution |
Coverage
- Active
- Listed
- Not covered
- European Union
- United States
Specification
- Generic Name
- Tooth extraction forceps
- Model / Reference
- Dental Device, F23IS
- Primary DI / UDI-DI
- 10889950113001
- Basic UDI-DI
- 0889950Hinged1RQN
- FDA Product Code
- EMG
- EMDN Code
- L150301 Dental extraction tooth forceps, reusable
- GMDN Term
- Tooth extraction forceps
- Device Class
- Class I
- Regulation Number
- 872.4565
- Market of Registration
- Germany
- Commercial Distribution
- In Commercial Distribution
Manufacturer details
- EUDAMED SRN
- US-MF-000017104
- Authorised representative
- Hu-Friedy Europe LLC & Co. KG DE-AR-000005530
Other devices from Hu-Friedy Manufacturing Co., LLC
Properties & raw data
Show properties, registry sources and raw records
Other properties (21)
- 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
- Prescription Use: 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 6e2c01ae-ec64-4ed9-a7ad-09831a4e063d
- FDA UDI 0c590dd6-1605-40ec-ba47-3a310d7e7f1d