Embrace™ Relief Wrap F00772

GUDID 00040337007723

Embrace™ Relief Wrap - Shoulder, Portable/Wearable Heat

Battle Creek Equipment Co.

Electric pad localized-body heating system

• Primary Device ID: 00040337007723
• NIH Device Record Key: 3058266a-c063-4d92-8c0f-ccd80ca682df
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Embrace™ Relief Wrap
• Version Model Number: Shoulder
• Catalog Number: F00772
• Company DUNS: 001957422
• Company Name: Battle Creek Equipment Co.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00040337007723 [Primary]

FDA Product Code

• IRT: Pad, Heating, Powered

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-12-22
• Device Publish Date: 2020-12-14

On-Brand Devices [Embrace™ Relief Wrap ]

• 00040337007730: Embrace™ Relief Wrap - Neck, Portable/Wearable Heat
• 00040337007723: Embrace™ Relief Wrap - Shoulder, Portable/Wearable Heat
• 00040337007716: Embrace™ Relief Wrap - Knee, Portable/Wearable Heat
• 00040337007709: Embrace™ Relief Wrap - Back, Portable/Wearable Heat