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BodyMed

FDA UDI

Class II (US FDA UDI)

by Boxout, Llc

Identity

Trade Name
BodyMed FDA UDI
Generic Name
External electric-heating core temperature regulation system pad FDA UDI
Device Name
BODYMED LED MOIST AND DRY HEATING PAD, WITH AUTO SHUT-OFF AT 2 HOURS. 12" X 15" FDA UDI
Model / Reference
ZZHP1215EA FDA UDI
Description
BODYMED LED MOIST AND DRY HEATING PAD, WITH AUTO SHUT-OFF AT 2 HOURS. 12" X 15" FDA UDI

Identifiers

Primary DI / UDI-DI
00815991024191 FDA UDI
FDA Product Code
IRT FDA UDI
GMDN Term
External electric-heating core temperature regulation system pad 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: External electric-heating core temperature regulation system pad

BodyMed by Boxout, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External electric-heating core temperature regulation system pad.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boxout, Llc

Sources (1)

  • FDA UDI 2aceb5a8-5d72-4b17-8e5e-cde33368059e 34 fields · synced May 30, 2026