BI-POLAR/ENDO PROVISIONAL SHELL 31-479563

GUDID 00880304319905

Biomet Orthopedics, LLC

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• Primary Device ID: 00880304319905
• NIH Device Record Key: c61452eb-95bf-4e67-a1c9-8c7900a73107
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BI-POLAR/ENDO PROVISIONAL SHELL
• Version Model Number: 31-479563
• Catalog Number: 31-479563
• 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: 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

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304319905 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K051569

FDA Product Code

• KWY: Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented

Sterilization

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

[00880304319905]

Moist Heat or Steam Sterilization

[00880304319905]

Moist Heat or Steam Sterilization

[00880304319905]

Moist Heat or Steam Sterilization

[00880304319905]

Moist Heat or Steam Sterilization

[00880304319905]

Moist Heat or Steam Sterilization

[00880304319905]

Moist Heat or Steam Sterilization

[00880304319905]

Moist Heat or Steam Sterilization

[00880304319905]

Moist Heat or Steam Sterilization

[00880304319905]

Moist Heat or Steam Sterilization

[00880304319905]

Moist Heat or Steam Sterilization

[00880304319905]

Moist Heat or Steam Sterilization

[00880304319905]

Moist Heat or Steam Sterilization

[00880304319905]

Moist Heat or Steam Sterilization

[00880304319905]

Moist Heat or Steam Sterilization

[00880304319905]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-02-07
• Device Publish Date: 2016-10-21

On-Brand Devices [BI-POLAR/ENDO PROVISIONAL SHELL]

• 00880304319936: 31-479568
• 00880304319929: 31-479565
• 00880304319905: 31-479563
• 00880304319882: 31-479561
• 00880304319851: 31-479558
• 00880304319820: 31-479555
• 00880304319806: 31-479553
• 00880304319783: 31-479551