LILLIPUT

GUDID 38033178100282

SORIN GROUP ITALIA SRL

Extracorporeal membrane oxygenator

• Primary Device ID: 38033178100282
• NIH Device Record Key: 1e218316-92c9-43f4-a332-77620175295d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LILLIPUT
• Version Model Number: D902 MODULE
• Company DUNS: 442126587
• Company Name: SORIN GROUP ITALIA SRL
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08033178100281 [Primary]
GS1	38033178100282 [Package]; Contains: 08033178100281; Package: BOX [5 Units]; In Commercial Distribution

FDA Product Code

• DTZ: OXYGENATOR, CARDIOPULMONARY BYPASS

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-01-22
• Device Publish Date: 2015-06-23

On-Brand Devices [LILLIPUT]

• 38033178100398: D902 PH.I.S.I.O.
• 38033178100381: D901 PH.I.S.I.O. + ADAPTORS
• 38033178100374: D902 CLOSED PH.I.S.I.O.
• 38033178100367: D901 CLOSED PH.I.S.I.O.
• 38033178100336: D902 MODULE PH.I.S.I.O.
• 38033178100329: D901 MODULE PH.I.S.I.O.
• 38033178100305: D902
• 38033178100282: D902 MODULE
• 38033178100275: D901 + ADAPTORS
• 38033178100268: D901 CLOSED
• 38033178100251: D901 MODULE