LINER PUSHER HEAD 423613

GUDID 00880304371736

Biomet Uk Ltd

Orthopaedic inorganic implant inserter/extractor, reusable

• Primary Device ID: 00880304371736
• NIH Device Record Key: 50eb6871-81a3-496d-a463-dc66a7c6e7c2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LINER PUSHER HEAD
• Version Model Number: 423613
• Catalog Number: 423613
• 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: 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

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 Identifiers

Device Issuing Agency	Device ID
GS1	00880304371736 [Primary]

FDA Product Code

• HXO: PUSHER, SOCKET

Sterilization

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

[00880304371736]

Moist Heat or Steam Sterilization

[00880304371736]

Moist Heat or Steam Sterilization

[00880304371736]

Moist Heat or Steam Sterilization

[00880304371736]

Moist Heat or Steam Sterilization

[00880304371736]

Moist Heat or Steam Sterilization

[00880304371736]

Moist Heat or Steam Sterilization

[00880304371736]

Moist Heat or Steam Sterilization

[00880304371736]

Moist Heat or Steam Sterilization

[00880304371736]

Moist Heat or Steam Sterilization

[00880304371736]

Moist Heat or Steam Sterilization

[00880304371736]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-09-11
• Device Publish Date: 2020-05-23

On-Brand Devices [LINER PUSHER HEAD]

• 00880304371767: 423616
• 00880304371736: 423613
• 00880304009387: 423614