LIFEPAK 20e Defibrillator/Monitors 96507-000006U

GUDID 00883873762356

USED ACLS LP20E CMM,PCNG,MNC,SPO2,EN

PHYSIO-CONTROL, INC.

Non-rechargeable professional semi-automated external defibrillator

• Primary Device ID: 00883873762356
• NIH Device Record Key: 51dbcd9b-f8a0-425b-8425-f783fb21abf1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LIFEPAK 20e Defibrillator/Monitors
• Version Model Number: 96507
• Catalog Number: 96507-000006U
• 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: false
• 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@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00883873762356 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P160026

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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-06-28
• Device Publish Date: 2024-06-20

On-Brand Devices [LIFEPAK 20e Defibrillator/Monitors]

• 00883873762400: USED ACLS LP20E CMM,PCNG,SPO2,EN
• 00883873762394: USED ACLS LP20E CMM,PCNG,ENG
• 00883873762356: USED ACLS LP20E CMM,PCNG,MNC,SPO2,EN