STEINMANN PIN/TROCAR POINT 950092

GUDID 00880304416581

Biomet Orthopedics, LLC

Orthopaedic bone wire

• Primary Device ID: 00880304416581
• NIH Device Record Key: b09379ae-3fd6-4463-93fc-65b0666df181
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: STEINMANN PIN/TROCAR POINT
• Version Model Number: 950092
• Catalog Number: 950092
• 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	00880304416581 [Primary]

FDA Product Code

• HWB: EXTRACTOR

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 [STEINMANN PIN/TROCAR POINT]

• 00880304609525: 32-362078
• 00880304609518: 32-361078
• 00880304416581: 950092