1.4mm K-Wire Tube

GUDID 07640187462227

The K-wire tubes are placed in the instrument trays (sterilization trays) and contain the Bonebridge K-wires.

Bonebridge AG

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• Primary Device ID: 07640187462227
• NIH Device Record Key: 798155f2-6822-486a-82e2-c5b89c56acaf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 1.4mm K-Wire Tube
• Version Model Number: B-410010
• Company DUNS: 480244832
• Company Name: Bonebridge AG
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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	07640187462227 [Primary]

FDA Product Code

• FSM: Tray, Surgical, Instrument

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-12-04
• Device Publish Date: 2023-11-24

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