Vanguard™ Knee System 32-422623

GUDID 00887868526589

Biomet Uk Ltd

Arthrodesis nail, non-sterile

• Primary Device ID: 00887868526589
• NIH Device Record Key: 27b7f440-5a11-4d79-98fe-998a3ff61f42
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vanguard™ Knee System
• Version Model Number: 32-422623
• Catalog Number: 32-422623
• Company DUNS: 219322575
• Company Name: Biomet Uk Ltd
• 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
• 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	00887868526589 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[00887868526589]

Moist Heat or Steam Sterilization

[00887868526589]

Moist Heat or Steam Sterilization

[00887868526589]

Moist Heat or Steam Sterilization

[00887868526589]

Moist Heat or Steam Sterilization

[00887868526589]

Moist Heat or Steam Sterilization

[00887868526589]

Moist Heat or Steam Sterilization

[00887868526589]

Moist Heat or Steam Sterilization

[00887868526589]

Moist Heat or Steam Sterilization

[00887868526589]

Moist Heat or Steam Sterilization

[00887868526589]

Moist Heat or Steam Sterilization

[00887868526589]

Moist Heat or Steam Sterilization

[00887868526589]

Moist Heat or Steam Sterilization

[00887868526589]

Moist Heat or Steam Sterilization

[00887868526589]

Moist Heat or Steam Sterilization

[00887868526589]

Moist Heat or Steam Sterilization

[00887868526589]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-06-21
• Device Publish Date: 2021-06-11

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