Medicon 51.79.05
by Medicon eG. Chirurgiemechaniker-Genossenschaft
Medicon 51.79.05 is a Class II device made by Medicon eG. Chirurgiemechaniker-Genossenschaft, listed in FDA GUDID since 13 Nov 2018 (UDI-DI 04046826063030), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04046826063030 | Date13 Nov 2018 | StatusListed |
Official records
- AccessGUDID record 04046826063030
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Medicon
- Generic name
- Urethrotome
- Model / Ref / Catalog
- 51.79.05
- Primary DI / UDI-DI
- 04046826063030
- FDA product code
- EZO
- GMDN term
- Urethrotome
- Device class
- Class II
- Regulation number
- 876.4770
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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