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Venus Viva

FDA UDI

Class II (US FDA UDI)

by Venus Concept Inc.

Identity

Trade Name
Venus Viva FDA UDI
Generic Name
Radio-frequency skin surface treatment system applicator FDA UDI
Model / Reference
VI102402GLB FDA UDI

Identifiers

Primary DI / UDI-DI
00810060830628 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Radio-frequency skin surface treatment system applicator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

Yes

FDA UDI

Over-the-Counter

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Radio-frequency skin/body contouring systemRadio-frequency skin surface treatment system applicator

Venus Viva by Venus Concept Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radio-frequency skin surface treatment system applicator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Venus Concept Inc.

Sources (1)

  • FDA UDI 0050cd31-3fed-4012-93fa-d5f4622f9bbc 32 fields · synced May 30, 2026