Bi-Metric XR™ Series Instrumentation X31-400212

GUDID 00887868512919

Biomet Orthopedics, LLC

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• Primary Device ID: 00887868512919
• NIH Device Record Key: f401cfdc-0942-48fa-82ea-5da7571a7dd1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bi-Metric XR™ Series Instrumentation
• Version Model Number: X31-400212
• Catalog Number: X31-400212
• 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
• 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 Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868512919 [Primary]

FDA Product Code

• LXH: Orthopedic manual surgical instrument

Sterilization

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

[00887868512919]

Moist Heat or Steam Sterilization

[00887868512919]

Moist Heat or Steam Sterilization

[00887868512919]

Moist Heat or Steam Sterilization

[00887868512919]

Moist Heat or Steam Sterilization

[00887868512919]

Moist Heat or Steam Sterilization

[00887868512919]

Moist Heat or Steam Sterilization

[00887868512919]

Moist Heat or Steam Sterilization

[00887868512919]

Moist Heat or Steam Sterilization

[00887868512919]

Moist Heat or Steam Sterilization

[00887868512919]

Moist Heat or Steam Sterilization

[00887868512919]

Moist Heat or Steam Sterilization

[00887868512919]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-05-16
• Device Publish Date: 2022-05-08

On-Brand Devices [Bi-Metric XR™ Series Instrumentation]

• 00887868512919: X31-400212
• 00887868512902: X31-400211
• 00887868512896: X31-400210