Beaty

GUDID 17290017875009

MEDICAL FEEDBACK TECHNOLOGIES LTD

Cardiopulmonary resuscitation feedback device, electronic

• Primary Device ID: 17290017875009
• NIH Device Record Key: c5fdc501-015f-4573-8fd5-6d79d5e77901
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Beaty
• Version Model Number: BE8789US
• Company DUNS: 532305866
• Company Name: MEDICAL FEEDBACK TECHNOLOGIES LTD
• 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: true
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290017875002 [Primary]
GS1	17290017875009 [Package]; Contains: 07290017875002; Package: [100 Units]; In Commercial Distribution

FDA Product Code

• PMJ: Cpr Aid Feedback Device (No Software)

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: 2019-04-04
• Device Publish Date: 2019-03-27