VANAGUARD DA360 SYSTEMTIBIAL TRIAL CASE 591302

GUDID 05019279451715

Biomet Uk Ltd

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• Primary Device ID: 05019279451715
• NIH Device Record Key: 4389b703-f7dc-4d22-b5af-253d1a6124fc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VANAGUARD DA360 SYSTEMTIBIAL TRIAL CASE
• Version Model Number: 591302
• Catalog Number: 591302
• 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: 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.c
• 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
• 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
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	05019279451715 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K093293

FDA Product Code

• JWH: PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

Sterilization

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

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

[05019279451715]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-26

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• 05019279150366 - Oxford® Instruments: 2023-05-03
• 05019279465972 - MAXIM KNEE INSTRUMENTATION: 2023-05-03
• 05019279466238 - AGC Knee System: 2023-05-03
• 05019279466887 - MAXIM KNEE INSTRUMENTATION: 2023-05-03
• 05019279467266 - MAXIM KNEE INSTRUMENTATION: 2023-05-03
• 05019279490004 - OXFORD UNICOMPARTMENTAL KNEE PHASE 3TIBIAL RESECTOR HEADLESS NAIL: 2023-05-03