GUIDE WIRE, BALL NOSE 1077

GUDID 00887868000072

Biomet Orthopedics, LLC

Orthopaedic bone wire

• Primary Device ID: 00887868000072
• NIH Device Record Key: 2af05e73-ee2d-47c9-b300-9f68a0dec159
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GUIDE WIRE, BALL NOSE
• Version Model Number: 1077
• Catalog Number: 1077
• 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

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868000072 [Primary]

FDA Product Code

• FZX: Guide, surgical, instrument

Sterilization

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

[00887868000072]

Moist Heat or Steam Sterilization

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