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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 DIGITAL MOIST HEATING PAD, 14" x 14" FDA UDI
Model / Reference
ZZHP1414 FDA UDI
Description
BODYMED DIGITAL MOIST HEATING PAD, 14" x 14" FDA UDI

Identifiers

Catalog Number
ZZHP1414 FDA UDI
Primary DI / UDI-DI
00815802010139 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 2b65d623-e6f5-4fbd-8916-4fa9fa4663d2 35 fields · synced May 31, 2026