PRIMOPAC CP0250

GUDID 20705032026137

MULTIPACK INF F5

CORDIS CORPORATION

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• Primary Device ID: 20705032026137
• NIH Device Record Key: 8dbd1747-7281-43fe-8f53-3c3c35fb50a8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PRIMOPAC
• Version Model Number: CP0250
• Catalog Number: CP0250
• Company DUNS: 806136177
• Company Name: CORDIS CORPORATION
• 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: 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	10705032026130 [Primary]
GS1	20705032026137 [Package]; Contains: 10705032026130; Package: Box [10 Units]; In Commercial Distribution

FDA Product Code

• DQO: Catheter, intravascular, diagnostic
• OEZ: Cardiovascular Procedure Kit

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: 2024-03-05
• Device Publish Date: 2024-02-26

On-Brand Devices [PRIMOPAC]

• 20705032076729: CP ST+ 6 JR4, JL4,PIG 145, CSI AVANTI, GW
• 20705032026137: MULTIPACK INF F5
• 20705032025680: PRIMOPACK INF F5
• 20705032025352: PRIMO PAC ST plus F5 W/CSI