LP RING LOC PROVISIONAL LINER 31-423557

GUDID 00880304311053

Biomet Orthopedics, LLC

Acetabulum prosthesis trial, reusable

• Primary Device ID: 00880304311053
• NIH Device Record Key: f815f66c-7af3-4895-b161-956d0e4e4124
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LP RING LOC PROVISIONAL LINER
• Version Model Number: 31-423557
• Catalog Number: 31-423557
• 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
• 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 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 Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304311053 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K920639

FDA Product Code

• JDI: Prosthesis, hip, semi-constrained, metal/polymer, cemented

Sterilization

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

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

Moist Heat or Steam Sterilization

[00880304311053]

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 [LP RING LOC PROVISIONAL LINER]

• 00880304311060: 31-423558
• 00880304311053: 31-423557
• 00880304311046: 31-423556
• 00880304311039: 31-423555
• 00880304311022: 31-423554
• 00880304311015: 31-423553
• 00880304311008: 31-423552
• 00880304311206: 31-423575
• 00880304311190: 31-423574
• 00880304311183: 31-423573
• 00880304311176: 31-423572
• 00880304311169: 31-423571
• 00880304311152: 31-423570
• 00880304311145: 31-423568
• 00880304311138: 31-423567
• 00880304311121: 31-423566
• 00880304311114: 31-423565
• 00880304311091: 31-423563
• 00880304311084: 31-423562
• 00880304311077: 31-423561
• 00880304310995: 31-423551