PERCEVAL PVS23

GUDID 08022057014702

DI for Perceval Size M

CORCYM SRL

Aortic heart valve bioprosthesis

• Primary Device ID: 08022057014702
• NIH Device Record Key: a7a4166c-ea20-4343-baea-4ee54d0ac17b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PERCEVAL
• Version Model Number: PVS23
• Catalog Number: PVS23
• Company DUNS: 441454802
• Company Name: CORCYM SRL
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• 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	08022057014702 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P150011

FDA Product Code

• LWR: Heart-Valve, Non-Allograft Tissue

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-05-19
• Device Publish Date: 2025-05-09

On-Brand Devices [PERCEVAL]

• 08022057014726: DI for Perceval Size XL
• 08022057014719: DI for Perceval Size L
• 08022057014702: DI for Perceval Size M
• 08022057014696: DI for Perceval Size S