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Poly Go

FDA UDI

Class N (US FDA UDI)

by Medtek Lighting Corp

Identity

Trade Name
Poly Go FDA UDI
Generic Name
Blue/red/infrared phototherapy lamp FDA UDI
Device Name
Handheld LED Light Therapy Device. Treatment heads, available in Red (633nm), Blue (415nm) and Infrared (850nm), help to mitigate a variety of skin conditions. There are 48 LEDs to provide a treatment area of 26 square cm. Battery powered with a charger. FDA UDI
Model / Reference
7000C FDA UDI
Description
Handheld LED Light Therapy Device. Treatment heads, available in Red (633nm), Blue (415nm) and Infrared (850nm), help to mitigate a variety of skin conditions. There are 48 LEDs to provide a treatment area of 26 square cm. Battery powered with a charger. FDA UDI

Identifiers

Primary DI / UDI-DI
B3437000C1 FDA UDI
FDA Product Code
PWC FDA UDI
GMDN Term
Blue/red/infrared phototherapy lamp FDA UDI

Classification

Device Class
N 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
MRI Safety
MR Conditional FDA UDI

Category: Blue/red/infrared phototherapy lamp

Poly Go by Medtek Lighting Corp — Class N — 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 ccb3242b-c72d-4d9a-87ad-756e706c5897 33 fields · synced Jun 1, 2026