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Heated Eye Pad Pro

FDA UDI

Class II (US FDA UDI)

by Digital Heat Corporation

Identity

Trade Name
Heated Eye Pad Pro FDA UDI
Generic Name
Eye heat therapy pack, reusable FDA UDI
Device Name
Ophthalmic warmer with timer FDA UDI
Model / Reference
Heated Eye Pad Pro FDA UDI
Description
Ophthalmic warmer with timer FDA UDI

Identifiers

Primary DI / UDI-DI
B172PRO0 FDA UDI
FDA Product Code
IRT FDA UDI
GMDN Term
Eye heat therapy pack, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5740 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

No

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: Eye heat therapy pack, reusable

Heated Eye Pad Pro by Digital Heat Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Eye heat therapy pack, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d8a29862-cbb4-4e26-9258-f092830e5c42 33 fields · synced Jun 6, 2026