MediMax Tech PMX42P ESU Plate
MediMax Tech PMX42P ESU Plate is a Class II device made by Medimax Tech Inc., cleared under FDA 510(k) K073360 on 19 Dec 2007 and listed in FDA GUDID since 11 May 2018 (UDI-DI 00817325022880), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00817325022880 | Date11 May 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK073360 | Date19 Dec 2007 | StatusActive |
Official records
- AccessGUDID record 00817325022880
- FDA 510(k) database K073360
Across registries
- FDA 510(k) K073360 decided 19 Dec 2007 Active
- FDA GUDID UDI-DI 00817325022880 listed 11 May 2018 Listed
Timeline
- Cleared FDA 510(k) K073360
- Listed FDA GUDID 00817325022880
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- MediMax Tech
- Generic name
- Electrosurgical return electrode, single-use
- Model / reference
- PMX42P ESU Plate
- Primary DI / UDI-DI
- 00817325022880
- 510(k) Number
- FDA product code
- GEI
- GMDN term
- Electrosurgical return electrode, single-use
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
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