Antmed TR2012
Antmed TR2012 is a Class II device made by ShenZhen Antmed Co., Ltd, listed in FDA GUDID since 24 Aug 2017 (UDI-DI 06945764404012), registry data as of 22 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 | Number06945764404012 | Date24 Aug 2017 | StatusListed |
Official records
- AccessGUDID record 06945764404012
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Antmed
- Generic name
- Angiographic syringe
- Model / reference
- TR2012
- Primary DI / UDI-DI
- 06945764404012
- FDA product code
- DXT
- GMDN term
- Angiographic syringe
- Device class
- Class II
- Regulation number
- 870.1650
- GUDID distribution status
- In Commercial Distribution
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