Tenor®

GUDID 00884450111956

BIOSPHERE MEDICAL

Peripheral vascular guidewire, manual

• Primary Device ID: 00884450111956
• NIH Device Record Key: 1f8f1974-790f-4f3d-8410-4286bd7aba65
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tenor®
• Version Model Number: 00884450111956
• Company DUNS: 635091932
• Company Name: BIOSPHERE MEDICAL
• 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

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Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450111956 [Primary]

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: 2018-03-29
• Device Publish Date: 2016-12-07

On-Brand Devices [Tenor®]

• 00884450111956: 00884450111956
• 00884450093658: 00884450093658
• 10884450093648: 00884450093641
• 10884450093662: 00884450093665