← Back to catalogue

Comfort Heal Heating Pad

FDA UDI

Class II (US FDA UDI)

by Home Aide Diagnostics, Inc.

Identity

Trade Name
Comfort Heal Heating Pad FDA UDI
Generic Name
Electric pad whole-body heating system FDA UDI
Device Name
12"x24" moist/dry electrical heating pad for household use. FDA UDI
Model / Reference
JY6101 FDA UDI
Description
12"x24" moist/dry electrical heating pad for household use. FDA UDI

Identifiers

Catalog Number
1034 FDA UDI
Primary DI / UDI-DI
00891237001034 FDA UDI
FDA Product Code
IRT FDA UDI
GMDN Term
Electric pad whole-body heating system 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electric pad whole-body heating system

Comfort Heal Heating Pad by Home Aide Diagnostics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electric pad whole-body heating system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 72457b78-99eb-4415-9d39-8a019b0efe3c 35 fields · synced Jun 8, 2026