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Wonder TDP Heat Lamp

FDA UDI

Class II (US FDA UDI)

by Prime Holly Corporation

Identity

Trade Name
Wonder TDP Heat Lamp FDA UDI
Generic Name
Musculoskeletal infrared phototherapy unit, non-wearable FDA UDI
Device Name
This lamp features a proprietary mineral plate to emit far infrared band FDA UDI
Model / Reference
L02 FDA UDI
Description
This lamp features a proprietary mineral plate to emit far infrared band FDA UDI

Identifiers

Primary DI / UDI-DI
00818318028162 FDA UDI
FDA Product Code
ILY FDA UDI
GMDN Term
Musculoskeletal infrared phototherapy unit, non-wearable 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

Yes

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

Category: Musculoskeletal infrared phototherapy unit, non-wearable

Wonder TDP Heat Lamp by Prime Holly Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Musculoskeletal infrared phototherapy unit, non-wearable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Prime Holly Corporation

Sources (1)

  • FDA UDI 9de84aec-fe18-407f-801d-fcda4b107098 34 fields · synced May 30, 2026