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Gillette Venus Silk Expert 3

FDA UDI

Class II (US FDA UDI)

by Procter & Gamble Manufacturing Company, The

Identity

Trade Name
Gillette Venus Silk Expert 3 FDA UDI
Generic Name
Cosmetic red-light phototherapy system, home-use FDA UDI
Device Name
Light Based Over-The-Counter Hair Removal FDA UDI
Model / Reference
BD3001 FDA UDI
Description
Light Based Over-The-Counter Hair Removal FDA UDI

Identifiers

Primary DI / UDI-DI
00069055879801 FDA UDI
FDA Product Code
OHT FDA UDI
GMDN Term
Cosmetic red-light phototherapy system, home-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cosmetic red-light phototherapy system, home-use

Gillette Venus Silk Expert 3 by Procter & Gamble Manufacturing Company, The — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cosmetic red-light phototherapy system, home-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9d3ebe76-1965-439e-a55a-cc471f8f8839 35 fields · synced May 30, 2026