HIPLOC™ SYSTEM 236055

GUDID 00887868214844

Biomet Uk Ltd

Orthopaedic bone screw, non-bioabsorbable, sterile

• Primary Device ID: 00887868214844
• NIH Device Record Key: 05225a69-4fa7-4da3-bc0c-f3d3c41d9a13
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HIPLOC™ SYSTEM
• Version Model Number: 236055
• Catalog Number: 236055
• Company DUNS: 219322575
• Company Name: Biomet Uk Ltd
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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

Device Dimensions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868214844 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K080685

FDA Product Code

• JDO: DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-10-09

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• 05019279466832 - MAXIM KNEE INSTRUMENTATION: 2024-09-11
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