PREMIER 32-484638

GUDID 00880304465497

Biomet Orthopedics, LLC

Bone punch, reusable

• Primary Device ID: 00880304465497
• NIH Device Record Key: a248d608-a712-4dcb-a0f1-f04c219a8e15
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PREMIER
• Version Model Number: 32-484638
• Catalog Number: 32-484638
• 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: 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 Identifiers

Device Issuing Agency	Device ID
GS1	00880304465497 [Primary]

FDA Product Code

• HWP: PUNCH, FEMORAL NECK

Sterilization

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

[00880304465497]

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 [PREMIER]

• 00880304465497: 32-484638
• 00880304464902: 32-484637
• 00880304434776: 32-487267
• 00880304434745: 32-487262
• 00880304434721: 32-487261
• 00880304434707: 32-487263
• 00880304434677: 32-487265
• 00880304434660: 32-487268
• 00880304434653: 32-487260
• 00880304434622: 32-487264
• 00880304434608: 32-487266