LUCAS™ CHEST COMPRESSION SYSTEM 99576-000043

GUDID 00883873861875

LUCAS 3, 3.0, IN SHIPPING BOX, EN

Jolife AB

Cardiac resuscitator, line-powered

• Primary Device ID: 00883873861875
• NIH Device Record Key: 0380cd62-385e-47c4-9d8b-2cad824059ef
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LUCAS™ CHEST COMPRESSION SYSTEM
• Version Model Number: 99576
• Catalog Number: 99576-000043
• 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	00883873861875 [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: 2016-11-14

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