Cordis PRECISE RX Nitinol Stent System P07030RXC

GUDID 20705032035306

CORDIS CORPORATION

Bare-metal carotid artery stent

• Primary Device ID: 20705032035306
• NIH Device Record Key: d2cafd5d-c0d6-4012-8cea-3950aab35cf3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cordis PRECISE RX Nitinol Stent System
• Version Model Number: P07030RXC
• Catalog Number: P07030RXC
• Company DUNS: 806136177
• Company Name: CORDIS CORPORATION
• 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: 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	20705032035306 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P030047

FDA Product Code

• NIM: STENT, CAROTID

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-02-11
• Device Publish Date: 2014-09-17

On-Brand Devices [Cordis PRECISE RX Nitinol Stent System]

• 20705032035610: P10020RXC
• 20705032035559: P09030RXC
• 20705032035528: P09020RXC
• 20705032035450: P08040RXC
• 20705032035429: P08030RXC
• 20705032035399: P08020RXC
• 20705032035337: P07040RXC
• 20705032035306: P07030RXC
• 20705032035276: P07020RXC
• 20705032035214: P06040RXC
• 20705032035184: P06030RXC
• 20705032035153: P06020RXC
• 20705032035092: P05040RXC
• 20705032035030: P05020RXC