VANGUARD(TM) INSTRUMENT 32-486210

GUDID 00880304349957

Biomet Orthopedics, LLC

Surgical mallet

• Primary Device ID: 00880304349957
• NIH Device Record Key: 16451ac9-f460-4eb3-973b-b93e70b5b47e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VANGUARD(TM) INSTRUMENT
• Version Model Number: 32-486210
• Catalog Number: 32-486210
• 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	00880304349957 [Primary]

FDA Product Code

• FZY: HAMMER, SURGICAL

Sterilization

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

[00880304349957]

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 [VANGUARD(TM) INSTRUMENT]

• 00880304443433: 32-488722
• 00880304443426: 32-488723
• 00880304441767: 32-485214
• 00880304349957: 32-486210
• 00880304612402: 32-485263
• 00880304443204: 32-485261
• 00880304443143: 32-485262
• 00880304441446: 32-486806
• 00880304441439: 32-486804
• 00880304439993: 32-485210
• 00880304439986: 32-485260