GUIDE WIRE, BALL NOSE 809230028

GUDID 00887868034671

Biomet Orthopedics, LLC

Orthopaedic bone wire

• Primary Device ID: 00887868034671
• NIH Device Record Key: 29845de8-5465-43f6-bf10-ce08238e9d15
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GUIDE WIRE, BALL NOSE
• Version Model Number: 8092-30-028
• Catalog Number: 809230028
• 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	00887868034671 [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, BALL NOSE]

• 00887868034688: 8092-30-038
• 00887868034671: 8092-30-028
• 00887868000072: 1077