Identity
- Trade Name
- Tenovi FDA UDI
- Generic Name
- Expiratory peak flow meter, analogue, reusable FDA UDI
- Device Name
- Tenovi Peak Flow Meter FDA UDI
- Model / Reference
- TC-PFM-A1 FDA UDI
- Description
- Tenovi Peak Flow Meter FDA UDI
Identifiers
- Primary DI / UDI-DI
- G004TCPFMA10 FDA UDI
- FDA Product Code
- BZH FDA UDI
- GMDN Term
- Expiratory peak flow meter, analogue, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.1860 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
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Expiratory peak flow meter, analogue, reusable
Tenovi by Tenovi Co — 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
- Tenovi Co
Sources (1)
- FDA UDI 5650e882-8178-4a6d-96e1-841916037050 33 fields · synced May 30, 2026