TAPERLOC COMPLETE MICRO PRIMARY FEMORAL 51-106100

GUDID 00880304514270

Biomet Orthopedics, LLC

Coated hip femur prosthesis, modular

• Primary Device ID: 00880304514270
• NIH Device Record Key: cbd8eeb6-53b1-4ad3-bf03-b5c3f1b63021
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TAPERLOC COMPLETE MICRO PRIMARY FEMORAL
• Version Model Number: 51-106100
• Catalog Number: 51-106100
• 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: 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
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00880304514270 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K110400

FDA Product Code

• KWH: PROSTHESIS, TOE, CONSTRAINED, POLYMER
• MEH: Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate

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: 2015-10-24

On-Brand Devices [TAPERLOC COMPLETE MICRO PRIMARY FEMORAL]

• 00880304515314: 51-108080
• 00880304515291: 51-108070
• 00880304515277: 51-108060
• 00880304515253: 51-108050
• 00880304515239: 51-108040
• 00880304514614: 51-106090
• 00880304514508: 51-106240
• 00880304514485: 51-106220
• 00880304514461: 51-106200
• 00880304514447: 51-106180
• 00880304514416: 51-106170
• 00880304514393: 51-106160
• 00880304514379: 51-106150
• 00880304514355: 51-106140
• 00880304514331: 51-106130
• 00880304514317: 51-106120
• 00880304514294: 51-106110
• 00880304514270: 51-106100
• 00880304513778: 51-107090
• 00880304513655: 51-107240
• 00880304513631: 51-107220
• 00880304513617: 51-107200
• 00880304513594: 51-107180
• 00880304513570: 51-107170
• 00880304513556: 51-107160
• 00880304513532: 51-107150
• 00880304513518: 51-107140
• 00880304513495: 51-107130
• 00880304513471: 51-107120
• 00880304513457: 51-107110
• 00880304513433: 51-107100
• 00880304513037: 51-109080
• 00880304513013: 51-109070
• 00880304512993: 51-109060
• 00880304512979: 51-109050