Mediplus 3651
Mediplus 3651 is a Class II device made by Mediplus, Ltd., listed in FDA GUDID since 16 Sep 2016 (UDI-DI 05055140701633), 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 | Number05055140701633 | Date16 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 05055140701633
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Mediplus
- Generic name
- Male urinary outflow analysis system cuff
- Model / reference
- 3651
- Primary DI / UDI-DI
- 05055140701633
- FDA product code
- FEN
- GMDN term
- Male urinary outflow analysis system cuff
- Device class
- Class II
- Regulation number
- 876.1620
- GUDID distribution status
- In Commercial Distribution
- Size
- Width — 38.0 Millimeter
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