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Vive

FDA UDI

Class II (US FDA UDI)

by Vive Health Llc

Identity

Trade Name
VIVE FDA UDI
Generic Name
Oxygen saturation/pulse rate electronic-signal simulator FDA UDI
Device Name
Pulse Oximeter FDA UDI
Model / Reference
DMD1049 FDA UDI
Description
Pulse Oximeter FDA UDI

Identifiers

Primary DI / UDI-DI
00810041981738 FDA UDI
FDA Product Code
DQA FDA UDI
GMDN Term
Oxygen saturation/pulse rate electronic-signal simulator 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

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: Oxygen saturation/pulse rate electronic-signal simulator

Vive by Vive Health Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oxygen saturation/pulse rate electronic-signal simulator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vive Health Llc

Sources (1)

  • FDA UDI 0e4a76c0-6a07-4515-850b-11d40d6a51b2 33 fields · synced May 30, 2026