MULTIPACK CP0215

GUDID 20705032025970

CUSTOM MULTIPACK F5.2 ST+

CORDIS CORPORATION

Angiographic catheter, single-use

• Primary Device ID: 20705032025970
• NIH Device Record Key: 0b9a1626-d4c7-4ef2-b031-16578819aaea
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MULTIPACK
• Version Model Number: CP0215
• Catalog Number: CP0215
• Company DUNS: 806136177
• Company Name: CORDIS CORPORATION
• 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	10705032025973 [Primary]
GS1	20705032025970 [Package]; Contains: 10705032025973; Package: Box [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K914007

FDA Product Code

• DQO: Catheter, intravascular, diagnostic

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: 2024-03-04
• Device Publish Date: 2024-02-23

On-Brand Devices [MULTIPACK]

• 20705032026496: MULTIPAC 5.2 ST+ JL4, JR4, PIG145 AND GW
• 20705032026472: CP INF 4 JL4, 3DRC, PIG145
• 20705032026328: MULTIPAC ST+ 5.2 JL4, AR, PIG, CSI, GW
• 20705032025970: CUSTOM MULTIPACK F5.2 ST+