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Platinum LED Therapy Lights

FDA UDI

Class II (US FDA UDI)

by Platinum Led Holdings Llc

Identity

Trade Name
Platinum LED Therapy Lights FDA UDI
Generic Name
Blue/red/infrared phototherapy lamp FDA UDI
Device Name
BIOMAX600 FDA UDI
Model / Reference
BIOMAX600 FDA UDI
Description
BIOMAX600 FDA UDI

Identifiers

Catalog Number
BIOMAX600 FDA UDI
Primary DI / UDI-DI
B842BIOMAX6000 FDA UDI
FDA Product Code
ILY FDA UDI
GMDN Term
Blue/red/infrared phototherapy lamp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5500 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

Yes

FDA UDI

Dimensions & Sizes

Size
Weight — 22 Pound FDA UDI

Category: Blue/red/infrared phototherapy lamp

Platinum LED Therapy Lights by Platinum Led Holdings Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blue/red/infrared phototherapy lamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 49301a53-d465-4c92-b8cd-b9f3eff8d7e6 37 fields · synced May 30, 2026