Identity
- Trade Name
- Telesis FDA UDI
- Generic Name
- Biofeedback system application software FDA UDI
- Device Name
- Telesis® Software for the Pathway® MR Series FDA UDI
- Model / Reference
- 9250 FDA UDI
- Description
- Telesis® Software for the Pathway® MR Series FDA UDI
Identifiers
- Catalog Number
- 9250 FDA UDI
- Primary DI / UDI-DI
- 00852423006080 FDA UDI
- FDA Product Code
- HCC FDA UDI
- GMDN Term
- Biofeedback system application software FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5050 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Biofeedback system application software
Telesis by Prometheus Group Of New Hampshire Limited, The — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Prometheus Group Of New Hampshire Limited, The
Sources (1)
- FDA UDI 99d307df-d0d1-4e97-b955-e816f3ebcf7d 35 fields · synced Jun 8, 2026