Electrocardiograph ECG-3F Plus
Electrocardiograph ECG-3F Plus is a Class II device made by Edan Instruments, Inc., listed in FDA GUDID since 22 Sep 2016 (UDI-DI 06944413807921), 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 | Number06944413807921 | Date22 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 06944413807921
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Electrocardiograph
- Generic name
- Electrocardiograph, professional, multichannel
- Model / reference
- ECG-3F Plus
- Primary DI / UDI-DI
- 06944413807921
- FDA product code
- DPS
- GMDN term
- Electrocardiograph, professional, multichannel
- Device class
- Class II
- Regulation number
- 870.2340
- GUDID distribution status
- In Commercial Distribution
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