LIFEPAK® 15 monitor/defibrillator 99577-000043

GUDID 00883873988053

15AABBABAABABAAAAAAAAAAALP15 MONITOR/DEFIB

PHYSIO-CONTROL, INC.

Physiologic-monitoring defibrillation system

• Primary Device ID: 00883873988053
• NIH Device Record Key: f889ec14-af89-45a6-8f62-614992e72455
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LIFEPAK® 15 monitor/defibrillator
• Version Model Number: 99577
• Catalog Number: 99577-000043
• 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: false
• 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	00883873988053 [Primary]

FDA Product Code

• MKJ: Automated external defibrillators (non-wearable)

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 [LIFEPAK® 15 monitor/defibrillator]

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