Guide Wire Pusher 110008500

GUDID 00887868463297

Biomet Orthopedics, LLC

Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable

• Primary Device ID: 00887868463297
• NIH Device Record Key: ac22341d-8d70-467b-a8c6-8f28f5f5e73b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Guide Wire Pusher
• Version Model Number: 110008500
• Catalog Number: 110008500
• 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: 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
• 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 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	00887868463297 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K140891

FDA Product Code

• HWC: Screw, fixation, bone

Sterilization

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

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

[00887868463297]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-03-31
• Device Publish Date: 2021-03-23

On-Brand Devices [Guide Wire Pusher]

• 00887868109867: 110008500
• 00887868109836: 110008493
• 00887868463297: 110008500
• 00887868463273: 110008493