← Back to catalogue

Vive

FDA UDI

Class I (US FDA UDI)

by Vive Health Llc

Identity

Trade Name
Vive FDA UDI
Generic Name
Assistive glove/mitten FDA UDI
Device Name
Elderly Restraint Mitten FDA UDI
Model / Reference
LVA3096 FDA UDI
Description
Elderly Restraint Mitten FDA UDI

Identifiers

Primary DI / UDI-DI
00810178883110 FDA UDI
FDA Product Code
FMQ FDA UDI
GMDN Term
Assistive glove/mitten FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6760 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 glove/mitten

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

Similar devices

Also classified as Assistive glove/mitten.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Vive Health Llc

Sources (1)

  • FDA UDI 5ec3ceb8-1f27-4813-bb25-750c33437a9c 33 fields · synced May 31, 2026