KIRSCHNERBORING WIRE 937512300

GUDID 00887868125072

Biomet Orthopedics, LLC

Orthopaedic bone wire

• Primary Device ID: 00887868125072
• NIH Device Record Key: 963c1a8a-6100-436f-af95-f9da26e742f9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KIRSCHNERBORING WIRE
• Version Model Number: 937512300
• Catalog Number: 937512300
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• 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: true
• 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

Customer Support Contacts

• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868125072 [Primary]

FDA Product Code

• HTY: PIN, FIXATION, SMOOTH

Sterilization

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

[00887868125072]

Moist Heat or Steam Sterilization

[00887868125072]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-10-14

On-Brand Devices [KIRSCHNERBORING WIRE]

• 00887868125195: 937520150
• 00887868125140: 937516150
• 00887868125126: 937515150
• 00887868125072: 937512300
• 00887868125065: 937512150
• 00887868125058: 937510150
• 00887868124983: 937508070