OSS SEGMENT TRIAL 110018649

GUDID 00880304678361

Biomet Orthopedics, LLC

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• Primary Device ID: 00880304678361
• NIH Device Record Key: 3253702f-38ff-4df3-bf6a-10b299242f99
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OSS SEGMENT TRIAL
• Version Model Number: 110018649
• Catalog Number: 110018649
• 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

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 Identifiers

Device Issuing Agency	Device ID
GS1	00880304678361 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K141331

FDA Product Code

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

Sterilization

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

[00880304678361]

Moist Heat or Steam Sterilization

[00880304678361]

Moist Heat or Steam Sterilization

[00880304678361]

Moist Heat or Steam Sterilization

[00880304678361]

Moist Heat or Steam Sterilization

[00880304678361]

Moist Heat or Steam Sterilization

[00880304678361]

Moist Heat or Steam Sterilization

[00880304678361]

Moist Heat or Steam Sterilization

[00880304678361]

Moist Heat or Steam Sterilization

[00880304678361]

Moist Heat or Steam Sterilization

[00880304678361]

Moist Heat or Steam Sterilization

[00880304678361]

Moist Heat or Steam Sterilization

[00880304678361]

Moist Heat or Steam Sterilization

[00880304678361]

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: 2016-10-27

On-Brand Devices [OSS SEGMENT TRIAL]

• 00880304678415: 110018654
• 00880304678408: 110018653
• 00880304678392: 110018652
• 00880304678385: 110018651
• 00880304678361: 110018649