Extension AG149001
Extension AG149001 is a Class II device made by Asahi Intecc Co., Ltd., listed in FDA GUDID since 24 Mar 2020 (UDI-DI 04547327083577), 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 | Number04547327083577 | Date24 Mar 2020 | StatusListed |
Official records
- AccessGUDID record 04547327083577
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Extension
- Generic name
- Coronary artery guidewire extension
- Model / reference
- AG149001
- Primary DI / UDI-DI
- 04547327083577
- FDA product code
- DQX
- GMDN term
- Coronary artery guidewire extension
- Device class
- Class II
- Regulation number
- 870.1330
- GUDID distribution status
- In Commercial Distribution
- Size
- Outer Diameter — 0.014 InchLength — 165 Centimeter
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