FIBULA COMPOSITE PLATE TRIAL 816307007

GUDID 00887868046094

Biomet Orthopedics, LLC

Surgical implant template, reusable

• Primary Device ID: 00887868046094
• NIH Device Record Key: 51a7e503-d1d7-42af-8ef0-63cc2e7db52a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FIBULA COMPOSITE PLATE TRIAL
• Version Model Number: 816307007
• Catalog Number: 816307007
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• 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

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868046094 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[00887868046094]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-06-26
• Device Publish Date: 2017-07-28

On-Brand Devices [FIBULA COMPOSITE PLATE TRIAL]

• 00887868046117: 816307014
• 00887868046100: 816307010
• 00887868046094: 816307007
• 00887868445866: 816307014
• 00887868445859: 816307010
• 00887868445842: 816307007