TrueCPR™ Coaching Device 80596-000003

GUDID 00883873890455

TRUECPR,PACKAGED,MULTI-LANGUAGE, CONFIG B

PHYSIO-CONTROL, INC.

Cardiopulmonary resuscitation feedback device, electronic

• Primary Device ID: 00883873890455
• NIH Device Record Key: abd7e219-fcc4-44dc-9b0d-3eebdecc9c93
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TrueCPR™ Coaching Device
• Version Model Number: 80596
• Catalog Number: 80596-000003
• Company DUNS: 009251992
• Company Name: PHYSIO-CONTROL, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@physio-control.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00883873890455 [Primary]

FDA Product Code

• LIX: AID, CARDIOPULMONARY RESUSCITATION

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2014-11-11

On-Brand Devices [TrueCPR™ Coaching Device]

• 00883873901045: TRUECPR, PACKAGED, MULTI-LANGUAGE
• 00883873890455: TRUECPR,PACKAGED,MULTI-LANGUAGE, CONFIG B