LUCAS CHEST COMPRESSION SYSTEM 11576-000080

GUDID 00883873861820

LUCAS BATTERY DARK GRAY

Jolife AB

Cardiac resuscitator, line-powered

• Primary Device ID: 00883873861820
• NIH Device Record Key: 4ef5f64b-2410-4ccd-ae64-d8acecacd84e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LUCAS CHEST COMPRESSION SYSTEM
• Version Model Number: 11576
• Catalog Number: 11576-000080
• Company DUNS: 632662933
• Company Name: Jolife AB
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• 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: false
• RX Perscription: false
• 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	00883873861820 [Primary]

FDA Product Code

• DRM: Compressor, cardiac, external

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-10-31
• Device Publish Date: 2016-11-14

On-Brand Devices [LUCAS CHEST COMPRESSION SYSTEM]

• 00883873861820: LUCAS BATTERY DARK GRAY
• 00883873826584: USED LUCAS 3, 3.0, IN SHIPPING BOX, EN
• 00883873826300: USED LUCAS 3, 3.1, IN SHIPPING BOX, EN