PRIMOPAC CP0138

GUDID 20705032025680

PRIMOPACK INF F5

CORDIS CORPORATION

Angiographic catheter, single-use

• Primary Device ID: 20705032025680
• NIH Device Record Key: 6574b6c0-2641-44b4-8de0-271ebe0aed11
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PRIMOPAC
• Version Model Number: CP0138
• Catalog Number: CP0138
• 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	10705032025683 [Primary]
GS1	20705032025680 [Package]; Contains: 10705032025683; 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