Loc 1012068-10
Loc 1012068-10 is a Class II device made by Abbott Vascular, listed in FDA GUDID since 5 Feb 2016 (UDI-DI 08717648124075), 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 | Number08717648124075 | Date5 Feb 2016 | StatusListed |
Official records
- AccessGUDID record 08717648124075
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Loc
- Generic name
- Peripheral vascular guidewire extension
- Model / Ref / Catalog
- 1012068-10
- Primary DI / UDI-DI
- 08717648124075
- FDA product code
- DQX
- GMDN term
- Peripheral vascular guidewire extension
- Device class
- Class II
- Regulation number
- 870.1330
- GUDID distribution status
- In Commercial Distribution
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