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Embrace™ Relief Wrap

FDA UDI

Class II (US FDA UDI)

by Battle Creek Equipment Co.

Identity

Trade Name
Embrace™ Relief Wrap FDA UDI
Generic Name
Electric pad localized-body heating system FDA UDI
Device Name
Embrace™ Relief Wrap - Shoulder, Portable/Wearable Heat FDA UDI
Model / Reference
Shoulder FDA UDI
Description
Embrace™ Relief Wrap - Shoulder, Portable/Wearable Heat FDA UDI

Identifiers

Catalog Number
F00772 FDA UDI
Primary DI / UDI-DI
00040337007723 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electric pad localized-body heating system

Embrace™ Relief Wrap by Battle Creek Equipment Co. — 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

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Manufacturer

Sources (1)

  • FDA UDI 3058266a-c063-4d92-8c0f-ccd80ca682df 34 fields · synced Jun 1, 2026