Jenx PL019 062
by Jenx Limited
Jenx PL019 062 is a Class I device made by Jenx Limited, listed in FDA GUDID since 29 Sep 2023 (UDI-DI 05056235212874), 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 | Number05056235212874 | Date29 Sep 2023 | StatusListed |
Official records
- AccessGUDID record 05056235212874
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Jenx
- Generic name
- Footrest
- Model / reference
- PL019 062
- Primary DI / UDI-DI
- 05056235212874
- FDA product code
- INW
- GMDN term
- Footrest
- Device class
- Class I
- Regulation number
- 890.3750
- GUDID distribution status
- In Commercial Distribution
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