MP TIBIAL TRAY CRUCIATE PUNCH 32-484521

GUDID 00880304612167

Biomet Orthopedics, LLC

Bone punch, reusable

• Primary Device ID: 00880304612167
• NIH Device Record Key: 96a7f4a7-ba26-4336-a6f9-95ee66231f9f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MP TIBIAL TRAY CRUCIATE PUNCH
• Version Model Number: 32-484521
• Catalog Number: 32-484521
• 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	00880304612167 [Primary]

FDA Product Code

• HWP: PUNCH, FEMORAL NECK

Sterilization

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

[00880304612167]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-07-28

On-Brand Devices [MP TIBIAL TRAY CRUCIATE PUNCH]

• 00880304612228: 32-484527
• 00880304612211: 32-484526
• 00880304612204: 32-484525
• 00880304612198: 32-484524
• 00880304612181: 32-484523
• 00880304612174: 32-484522
• 00880304612167: 32-484521