Identity
- Trade Name
- TeleRPM FDA UDI
- Generic Name
- Pulse oximeter FDA UDI
- Model / Reference
- TRK01 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850042929445 FDA UDI
- GMDN Term
- Pulse oximeter FDA UDI
Classification
- 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
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Pulse oximeter
TeleRPM by Mio Labs Inc. — 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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Mio Labs Inc.
Sources (1)
- FDA UDI 8299b771-47bd-48e9-a6a6-13d07276d0e1 32 fields · synced Jun 1, 2026