← Back to catalogue

Homedics

FDA UDI

Class II (US FDA UDI)

by Fka Distributing Co., Llc

Identity

Trade Name
HOMEDICS FDA UDI
Generic Name
Electric pad localized-body heating system FDA UDI
Device Name
"12"X15"GEL HEATING PAD FDA UDI
Model / Reference
HP-G50DSJ-2 FDA UDI
Description
"12"X15"GEL HEATING PAD FDA UDI

Identifiers

Primary DI / UDI-DI
00031262113900 FDA UDI
FDA Product Code
IRT FDA UDI
GMDN Term
Electric pad localized-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 localized-body heating system

Homedics by Fka Distributing Co., Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electric pad localized-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 4685fc2c-3c7f-4d9c-8afb-1cc8dd19a87b 33 fields · synced Jun 8, 2026