← Back to catalogue

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 - Back, Portable/Wearable Heat FDA UDI
Model / Reference
Back FDA UDI
Description
Embrace™ Relief Wrap - Back, Portable/Wearable Heat FDA UDI

Identifiers

Catalog Number
F00770 FDA UDI
Primary DI / UDI-DI
00040337007709 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

Relieve pain and discomfort with the Embrace Relief Wrap, a portable and wearable heat therapy device designed for back and localized body site applications. This medical-grade, AC-powered electric heating pad is engineered to provide targeted warmth and comfort to sensitive areas, promoting relaxation and reducing muscle tension.

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

Manufacturer
Battle Creek Equipment Co.

Sources (1)

  • FDA UDI 0c975fc3-4b6d-47f6-8ce3-94856c234d8b 34 fields · synced Jul 3, 2026