Namic 80485003
Namic 80485003 is a Class II device made by Medline Industries, Inc., listed in FDA GUDID since 3 Jun 2021 (UDI-DI 30193489067044), 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 | Number30193489067044 | Date3 Jun 2021 | StatusListed |
Official records
- AccessGUDID record 30193489067044
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Namic
- Generic name
- Torque manipulation device
- Model / Ref / Catalog
- 80485003
- Primary DI / UDI-DI
- 30193489067044
- FDA product code
- DQX
- 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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