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Trophy Skin

FDA UDI

Class II (US FDA UDI)

by Trophy Skin, Inc.

Identity

Trade Name
Trophy Skin FDA UDI
Generic Name
Skin photodynamic therapy/phototherapy lamp FDA UDI
Device Name
BlueMD, Blue Light Therapy Device FDA UDI
Model / Reference
BlueMD FDA UDI
Description
BlueMD, Blue Light Therapy Device FDA UDI

Identifiers

Primary DI / UDI-DI
00851561006020 FDA UDI
FDA Product Code
MXG FDA UDI
GMDN Term
Skin photodynamic therapy/phototherapy lamp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4630 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Skin photodynamic therapy/phototherapy lamp

Trophy Skin by Trophy Skin, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin photodynamic therapy/phototherapy lamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Trophy Skin, Inc.

Sources (1)

  • FDA UDI 38f7a5a7-6a78-4c59-a52b-47f47d5d8fa1 34 fields · synced May 31, 2026