Perceval S Single Use Accessory Kit

GUDID 08022057015204

SORIN GROUP ITALIA SRL

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• Primary Device ID: 08022057015204
• NIH Device Record Key: 6d48536a-74ff-4071-b052-6b224db0e848
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Perceval S Single Use Accessory Kit
• Version Model Number: ICV1345
• Company DUNS: 428011907
• 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: true
• 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	08022057015204 [Primary]

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: 2019-04-23
• Device Publish Date: 2016-06-06

On-Brand Devices [Perceval S Single Use Accessory Kit]

• 08022057015242: ICV1348
• 08022057015235: ICV1347
• 08022057015228: ICV1346
• 08022057015204: ICV1345