Primus 9275
by Prometheus Group of New Hampshire Limited, the
Primus 9275 is a Class II device made by Prometheus Group of New Hampshire Limited, the, listed in FDA GUDID since 26 Sep 2016 (UDI-DI 00852423006097), 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 | Number00852423006097 | Date26 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00852423006097
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Primus
- Generic name
- Biofeedback system application software
- Model / Ref / Catalog
- 9275
- Primary DI / UDI-DI
- 00852423006097
- FDA product code
- HCC
- GMDN term
- Biofeedback system application software
- Device class
- Class II
- Regulation number
- 882.5050
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code HCC (Device, Biofeedback).
- EMG-UT 30 by American Scientific Corp.
- APOLLO HEART RATE INDICATOR by Key Tronic Corp.
- REGAIN DESKTOP by SRS Medical Systems, Inc.
- POLYGRAM NET BIOFEEDBACK APPLICATION by MEDTRONIC VASCULAR, INC.
- MyOnyx Mobile App SA9030 by Thought Technology Ltd.
- RELAX STRESS REDUCTION SYS by Synapse Software Corp.
- PROFESSIONAL SERIES BIOFEEDBACK DEVICES MODEL 421 by Self Regulation Systems, Inc.
- MODEL MES-9000/EMG SYSTEM by MYOTRONICS-NOROMED, INC.
- BRAINMASTER 2E MODULE AND SOFTWARE BIOFEEDBACK DEVICE by Brainmaster
- MINIATURE ELECTRODERMAL RESPONSE TRAINER EDR-002 by Bio-Feedback Systems, Inc.
Other devices from Prometheus Group of New Hampshire Limited, the
See all devices from Prometheus Group of New Hampshire Limited, the →