TISSUE PROBE 994500111

GUDID 00880304428218

Biomet Orthopedics, LLC

Surgical implant template, reusable

• Primary Device ID: 00880304428218
• NIH Device Record Key: ed4d0a69-c465-49ae-ab7e-f44f2dce08c3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TISSUE PROBE
• Version Model Number: 994500111
• Catalog Number: 994500111
• 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	00880304428218 [Primary]

FDA Product Code

• HXB: PROBE

Sterilization

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

[00880304428218]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-06-26
• Device Publish Date: 2017-07-28

On-Brand Devices [TISSUE PROBE]

• 00880304428218: 994500111
• 00887868561153: 994500111