FIRMap AR064050
by Abbott
FIRMap AR064050 is a Class II device made by Abbott, listed in FDA GUDID since 2 Sep 2016 (UDI-DI 00810591020017), 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 | Number00810591020017 | Date2 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00810591020017
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- FIRMap
- Generic name
- Cardiac mapping catheter, percutaneous, single-use
- Model / Ref / Catalog
- AR064050
- Primary DI / UDI-DI
- 00810591020017
- FDA product code
- MTD
- GMDN term
- Cardiac mapping catheter, percutaneous, single-use
- Device class
- Class II
- Regulation number
- 870.1220
- GUDID distribution status
- In Commercial Distribution
- Size
- Circumference — 50 Millimeter
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