Identity
- Trade Name
- MOBI FDA UDI
- Generic Name
- Pulse oximeter, line-powered FDA UDI
- Device Name
- MOBI’s Fingertip Pulse Oximeter offers a noninvasive method for monitoring oxygen salutation. Though its reading of peripheral oxygen saturation (SPO2). It is portable, lightweight and multi-functional that can perform the measurement within 10 seconds. FDA UDI
- Model / Reference
- 70299 FDA UDI
- Description
- MOBI’s Fingertip Pulse Oximeter offers a noninvasive method for monitoring oxygen salutation. Though its reading of peripheral oxygen saturation (SPO2). It is portable, lightweight and multi-functional that can perform the measurement within 10 seconds. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00891040702999 FDA UDI
- 510(k) Number
- K173123 FDA UDI
- FDA Product Code
- DQA FDA UDI
- GMDN Term
- Pulse oximeter, line-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2700 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: Pulse oximeter, line-powered
Mobi by Mobi Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K173123 also covers:
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
- Mobi Technologies, Inc.
Sources (1)
- FDA UDI 95a5f9e5-c2b3-4b3e-8e95-0b1615e431b4 35 fields · synced May 30, 2026