LUCAS™ Chest Compression System 99576-000024

GUDID 00883873904565

LUCAS 2, 2.2, IN SHIPPING BOX,EN

Jolife AB

Cardiac resuscitator, line-powered

• Primary Device ID: 00883873904565
• NIH Device Record Key: c6eebe8f-4c78-47b6-baba-5f0ee3c3cc6b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LUCAS™ Chest Compression System
• Version Model Number: 99576
• Catalog Number: 99576-000024
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• 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	00883873904565 [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: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2014-12-04

On-Brand Devices [LUCAS™ Chest Compression System]

• 00883873904565: LUCAS 2, 2.2, IN SHIPPING BOX,EN
• 00883873861875: LUCAS 3, 3.0, IN SHIPPING BOX, EN