Taperloc® Microplasty® Complete 51-208060

GUDID 00887868508752

Biomet Orthopedics, LLC

Bone file/rasp, manual

• Primary Device ID: 00887868508752
• NIH Device Record Key: 796f24ff-5639-46ce-8d70-440840178de3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Taperloc® Microplasty® Complete
• Version Model Number: 51-208060
• Catalog Number: 51-208060
• 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

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 Identifiers

Device Issuing Agency	Device ID
GS1	00887868508752 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K110400

FDA Product Code

• KWL: Prosthesis, hip, hemi-, femoral, metal

Sterilization

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

[00887868508752]

Moist Heat or Steam Sterilization

[00887868508752]

Moist Heat or Steam Sterilization

[00887868508752]

Moist Heat or Steam Sterilization

[00887868508752]

Moist Heat or Steam Sterilization

[00887868508752]

Moist Heat or Steam Sterilization

[00887868508752]

Moist Heat or Steam Sterilization

[00887868508752]

Moist Heat or Steam Sterilization

[00887868508752]

Moist Heat or Steam Sterilization

[00887868508752]

Moist Heat or Steam Sterilization

[00887868508752]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-06-02
• Device Publish Date: 2022-05-25

On-Brand Devices [Taperloc® Microplasty® Complete]

• 00887868508776: 51-208080
• 00887868508769: 51-208070
• 00887868508752: 51-208060
• 00887868508745: 51-208050
• 00887868508738: 51-208040
• 00887868508721: 51-206240
• 00887868508714: 51-206220
• 00887868508707: 51-206200
• 00887868508691: 51-206180
• 00887868508684: 51-206170
• 00887868508677: 51-206160
• 00887868508660: 51-206150
• 00887868508653: 51-206140
• 00887868508646: 51-206130
• 00887868508639: 51-206120
• 00887868508622: 51-206110
• 00887868508615: 51-206100
• 00887868508608: 51-206090