A.L.P.S.MIS TARGETING GUIDE 110008305

GUDID 00887868076619

Biomet Orthopedics, LLC

Orthopaedic implant aiming/guiding block, reusable

• Primary Device ID: 00887868076619
• NIH Device Record Key: 7af75d41-2f80-4df9-9753-2b2de4423bdd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: A.L.P.S.MIS TARGETING GUIDE
• Version Model Number: 110008305
• Catalog Number: 110008305
• 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

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868076619 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K132898

FDA Product Code

• HRS: Plate, fixation, bone

Sterilization

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

[00887868076619]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-26

On-Brand Devices [A.L.P.S.MIS TARGETING GUIDE]

• 00887868076626: 110008307
• 00887868076619: 110008305
• 00887868076602: 110008303
• 00887868076596: 110008301