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Vive Mobility

FDA UDI

Class II (US FDA UDI)

by Vive Health Llc

Identity

Trade Name
Vive Mobility FDA UDI
Generic Name
Assistive scooter, electric-motor-driven FDA UDI
Device Name
4 Wheel Mobility Scooter (Silver) FDA UDI
Model / Reference
MOB1027SLV FDA UDI
Description
4 Wheel Mobility Scooter (Silver) FDA UDI

Identifiers

Primary DI / UDI-DI
00818323027976 FDA UDI
FDA Product Code
INI FDA UDI
GMDN Term
Assistive scooter, electric-motor-driven FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3800 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: Assistive scooter, electric-motor-driven

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

Similar devices

Also classified as Assistive scooter, electric-motor-driven.

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 b6a780a5-e77c-4fa9-bd81-8da0e05ee254 33 fields · synced Jun 8, 2026