Guidewire GW35180

GUDID 00885672101466

Guidewire with PTFE coating

Oscor Inc.

Peripheral vascular guidewire, manual

• Primary Device ID: 00885672101466
• NIH Device Record Key: c53d9a15-7601-470f-93e0-937b71ee0110
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Guidewire
• Version Model Number: GW35180
• Catalog Number: GW35180
• Company DUNS: 101835833
• Company Name: Oscor Inc.
• 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: 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

Customer Support Contacts

• Phone: +1(727)937-2511
• Email: sales@oscor.com
• Phone: +1(727)937-2511
• Email: sales@oscor.com
• Phone: +1(727)937-2511
• Email: sales@oscor.com
• Phone: +1(727)937-2511
• Email: sales@oscor.com
• Phone: +1(727)937-2511
• Email: sales@oscor.com
• Phone: +1(727)937-2511
• Email: sales@oscor.com
• Phone: +1(727)937-2511
• Email: sales@oscor.com
• Phone: +1(727)937-2511
• Email: sales@oscor.com
• Phone: +1(727)937-2511
• Email: sales@oscor.com
• Phone: +1(727)937-2511
• Email: sales@oscor.com
• Phone: +1(727)937-2511
• Email: sales@oscor.com
• Phone: +1(727)937-2511
• Email: sales@oscor.com
• Phone: +1(727)937-2511
• Email: sales@oscor.com
• Phone: +1(727)937-2511
• Email: sales@oscor.com
• Phone: +1(727)937-2511
• Email: sales@oscor.com
• Phone: +1(727)937-2511
• Email: sales@oscor.com
• Phone: +1(727)937-2511
• Email: sales@oscor.com
• Phone: +1(727)937-2511
• Email: sales@oscor.com

Device Dimensions

• Outer Diameter: 0.035 Inch
• Length: 180 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 180 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 180 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 180 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 180 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 180 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 180 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 180 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 180 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 180 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 180 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 180 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 180 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 180 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 180 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 180 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 180 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 180 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885672101466 [Primary]

FDA Product Code

• DQX: Wire, guide, catheter

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: 2023-09-15
• Device Publish Date: 2023-09-07

On-Brand Devices [Guidewire]

• 00885672010010: Guidewire with PTFE coating
• 00885672101466: Guidewire with PTFE coating