Namic 80485003
Namic 80485003 is a Class II device made by Navilyst Medical, Inc., listed in FDA GUDID since 17 Sep 2015 (UDI-DI H749804850030), registry data as of 23 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 | NumberH749804850030 | Date17 Sep 2015 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Namic
- Generic name
- Torque manipulation device
- Model / reference
- 80485003
- Primary DI / UDI-DI
- H749804850030
- FDA product code
- DQX, PTL
- GMDN term
- Torque manipulation device
- Device class
- Class II
- Regulation number
- 870.1330
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Ethylene Oxide
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