Inspire

GUDID 08033178111966

SORIN GROUP ITALIA SRL

Medical device service rail clamp

• Primary Device ID: 08033178111966
• NIH Device Record Key: 7ef8b44f-6cfb-4b1a-b34a-3f157d30213b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Inspire
• Version Model Number: Bracket
• Company DUNS: 442126587
• Company Name: SORIN GROUP ITALIA SRL
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Serial Number: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	08033178111966 [Primary]

FDA Product Code

• KRI: ACCESSORY EQUIPMENT, CARDIOPULMONARY BYPASS

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-11-01
• Device Publish Date: 2023-10-24

On-Brand Devices [Inspire]

• 38033178113237: 7 DUAL
• 38033178113213: 7
• 38033178113183: 7 M
• 38033178113015: SVR 1200
• 38033178112421: 8F DUAL PH.I.S.I.O.
• 38033178112414: 6F DUAL PH.I.S.I.O.
• 38033178112407: 8 DUAL PH.I.S.I.O.
• 38033178112391: 6 DUAL PH.I.S.I.O.
• 38033178112384: 8F PH.I.S.I.O.
• 38033178112377: 6F PH.I.S.I.O.
• 38033178112360: 8 PH.I.S.I.O.
• 38033178112353: 6 PH.I.S.I.O.
• 38033178112308: HVR DUAL
• 38033178112292: HVR
• 38033178112285: 8F M
• 38033178112278: 6F M
• 38033178112261: 8M
• 38033178112254: 6M
• 38033178113367: 7F DUAL
• 38033178113350: 7F
• 38033178113343: 7F M
• 08033178112994: Bracket
• 08033178112987: Bracket 1200
• 08033178112970: Bracket
• 08033178111966: Bracket
• 08033178111959: Bracket