GUIDE WIRE 809232228

GUDID 00887868034695

Biomet Orthopedics, LLC

Orthopaedic bone wire

• Primary Device ID: 00887868034695
• NIH Device Record Key: afe98065-c2e1-4e20-83e3-49794e28bc08
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GUIDE WIRE
• Version Model Number: 8092-32-228
• Catalog Number: 809232228
• 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: 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(800)348-9500
• Email: customerservice@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868034695 [Primary]

FDA Product Code

• FZX: Guide, surgical, instrument

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: 2024-02-19
• Device Publish Date: 2020-05-23

On-Brand Devices [GUIDE WIRE]

• 00887868005251: 1724-28
• 00887868004001: 14012-9
• 00887868510700: 8092-22-028
• 70887868004000: 14012-9
• 00880304415959: 945020
• 00887868556876: 909894
• 00887868034701: 8092-32-238
• 00887868034695: 8092-32-228
• 00887868034664: 8092-22-028
• 00887868003936: 1075-38
• 00887868003929: 1075-28