LIFEPAK 1000 LiMnO2 non rechargeable battery 11141-000100

GUDID 00885074503592

ASSEMBLY BATTERY REPLACEMENT KIT

PHYSIO-CONTROL, INC.

Primary battery

• Primary Device ID: 00885074503592
• NIH Device Record Key: 5a85008b-2904-4dde-8fed-c2de382f4e67
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LIFEPAK 1000 LiMnO2 non rechargeable battery
• Version Model Number: 11141
• Catalog Number: 11141-000100
• 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: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885074503592 [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: 2014-11-10

On-Brand Devices [LIFEPAK 1000 LiMnO2 non rechargeable battery]

• 00885074503592: ASSEMBLY BATTERY REPLACEMENT KIT
• 00883873919477: ASSY-BATTERY,PRIMARY,5/4C CELL,LIMN02,LP1000