Novaplus V02-400-030
Novaplus V02-400-030 is a Class II device made by Next Medical Products, LLC, listed in FDA GUDID since 12 Jun 2023 (UDI-DI 30856724004524), registry data as of 8 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number30856724004524 | Date12 Jun 2023 | StatusListed |
Official records
- AccessGUDID record 30856724004524
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Novaplus
- Generic name
- Skin topical coupling gel
- Model / reference
- V02-400-030
- Primary DI / UDI-DI
- 30856724004524
- FDA product code
- IYO
- GMDN term
- Skin topical coupling gel
- Device class
- Class II
- Regulation number
- 892.1560
- GUDID distribution status
- In Commercial Distribution
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