OXFORD LATERAL INSTRUMENTS 32-423350

GUDID 00880304609945

Biomet Orthopedics, LLC

Manual bone mill

• Primary Device ID: 00880304609945
• NIH Device Record Key: 0cbe3cb7-0667-4fdb-a9ea-283878367aa8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OXFORD LATERAL INSTRUMENTS
• Version Model Number: 32-423350
• Catalog Number: 32-423350
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00880304609945 [Primary]

FDA Product Code

• HWT: TEMPLATE

Sterilization

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

[00880304609945]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-10-05
• Device Publish Date: 2017-07-28

On-Brand Devices [OXFORD LATERAL INSTRUMENTS]

• 00880304609952: 32-423353
• 00880304609945: 32-423350
• 00880304609884: 32-423339
• 00880304543560: 32-423352
• 00880304543553: 32-423351
• 00880304543546: 32-423341
• 00880304543539: 32-423343
• 00880304543522: 32-423344
• 00880304543478: 32-423342
• 00880304543447: 32-423340
• 00880304543430: 32-423337
• 00880304543423: 32-423338