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Future Generation Medical

FDA UDI

Class I (US FDA UDI)

by Global International L. L. C.

Identity

Trade Name
Future Generation Medical FDA UDI
Generic Name
Exothermic heat therapy pack/patch FDA UDI
Device Name
Foot Warmer(10h) / Small FDA UDI
Model / Reference
FGFW-8119A FDA UDI
Description
Foot Warmer(10h) / Small FDA UDI

Identifiers

Primary DI / UDI-DI
10850046230230 FDA UDI
FDA Product Code
OMW FDA UDI
GMDN Term
Exothermic heat therapy pack/patch FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5710 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

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Exothermic heat therapy pack/patch

Future Generation Medical by Global International L. L. C. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Exothermic heat therapy pack/patch.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 651a5bc4-509f-44cf-abca-5bd7d237dba1 34 fields · synced Jun 6, 2026