SPECTRE 7387

GUDID 30841156101149

Spectre Guidewire 300cm

TELEFLEX INCORPORATED

Cardiac/peripheral vascular guidewire, single-use

• Primary Device ID: 30841156101149
• NIH Device Record Key: dac341cd-ae2c-4bc5-bad5-8417fece7ecd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SPECTRE
• Version Model Number: IPN913605
• Catalog Number: 7387
• Company DUNS: 002348191
• Company Name: TELEFLEX INCORPORATED
• 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: true
• 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

Customer Support Contacts

• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM

Device Dimensions

• Length: 300 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	10841156101145 [Primary]
GS1	30841156101149 [Package]; Contains: 10841156101145; Package: Box [5 Units]; In Commercial Distribution

FDA Product Code

• DQX: Wire, guide, catheter

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-11-11
• Device Publish Date: 2019-01-22

On-Brand Devices [SPECTRE]

• 30841156101132: Spectre Guidewire 190cm
• 30841156101149: Spectre Guidewire 300cm
• 20841156106505: Spectre guidewire, 200cm
• 20841156108028: Spectre Guidewire, 300cm
• 20841156108011: Spectre Guidewire, 200cm
• 20841156111424: Spectre Guidewire 300CM
• 20841156111417: IPN930527