Beaty

Basic Information

• Brand Name: Beaty
• Primary DI: 07290017875002
• Version / Model: BE8789US
• Company Name: MEDICAL FEEDBACK TECHNOLOGIES LTD
• Labeler DUNS: 532305866
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2019-03-27
• Public Version: 1
• Public Version Date: 2019-04-04
• Public Version Status: New
• Public Device Record Key: c5fdc501-015f-4573-8fd5-6d79d5e77901

Device Characteristics

• Single Use: No
• Prescription Use (Rx): No
• Over the Counter (OTC): Yes
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: Yes
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: Yes
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
PMJ	Cpr Aid Feedback Device (No Software)	Cardiovascular	870.5210	2

GMDN Terms

Code	Name	Definition	Implantable	Status
60368	Cardiopulmonary resuscitation feedback device, electronic	A portable, battery-powered device intended to provide real-time feedback on manual chest compressions (i.e., depth of compression) performed during cardiopulmonary resuscitation (CPR) on a patient in cardiac arrest, or during training on a resuscitation training model. It typically consists of a chest plate with a digital display, which is placed on the sternum and pushed down during chest compressions and will display compression depth and rate, measured by one of various electronic technologies (e.g., electromagnetic signaling to a baseplate, accelerometer). It is intended to be used by those trained in CPR.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Package	17290017875009	GS1		100	In Commercial Distribution
Primary	07290017875002	GS1