Vanguard 360® Instrument 32-488474

GUDID 00887868497124

Biomet Orthopedics, LLC

Medullary canal orthopaedic reamer, flexible

• Primary Device ID: 00887868497124
• NIH Device Record Key: 9d0639e0-096c-4d3c-9212-bd85f81ec7df
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vanguard 360® Instrument
• Version Model Number: 32-488474
• Catalog Number: 32-488474
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868497124 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K093293

FDA Product Code

• MBV: Prosthesis, knee, patello/femorotibial, semi-constrained, uhmwpe, pegged, cemented, polymer/metal/polymer

Sterilization

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

[00887868497124]

Moist Heat or Steam Sterilization

[00887868497124]

Moist Heat or Steam Sterilization

[00887868497124]

Moist Heat or Steam Sterilization

[00887868497124]

Moist Heat or Steam Sterilization

[00887868497124]

Moist Heat or Steam Sterilization

[00887868497124]

Moist Heat or Steam Sterilization

[00887868497124]

Moist Heat or Steam Sterilization

[00887868497124]

Moist Heat or Steam Sterilization

[00887868497124]

Moist Heat or Steam Sterilization

[00887868497124]

Moist Heat or Steam Sterilization

[00887868497124]

Moist Heat or Steam Sterilization

[00887868497124]

Moist Heat or Steam Sterilization

[00887868497124]

Moist Heat or Steam Sterilization

[00887868497124]

Moist Heat or Steam Sterilization

[00887868497124]

Moist Heat or Steam Sterilization

[00887868497124]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-04-04
• Device Publish Date: 2022-03-26

On-Brand Devices [Vanguard 360® Instrument]

• 00887868497124: 32-488474
• 00887868497117: 32-488473
• 00887868497100: 32-488472
• 00887868497094: 32-488471
• 00887868497087: 32-488470
• 00887868497070: 32-488428
• 00887868496547: 32-487559