Vanguard® 360 Instrument 32-360095

GUDID 00887868562310

Biomet Orthopedics, LLC

Orthopaedic prosthesis implantation positioning instrument, reusable

• Primary Device ID: 00887868562310
• NIH Device Record Key: 7ef7a36f-43e4-4fcb-a116-cc5c27473a97
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vanguard® 360 Instrument
• Version Model Number: 32-360095
• Catalog Number: 32-360095
• 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
• 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 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	00887868562310 [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

[00887868562310]

Moist Heat or Steam Sterilization

[00887868562310]

Moist Heat or Steam Sterilization

[00887868562310]

Moist Heat or Steam Sterilization

[00887868562310]

Moist Heat or Steam Sterilization

[00887868562310]

Moist Heat or Steam Sterilization

[00887868562310]

Moist Heat or Steam Sterilization

[00887868562310]

Moist Heat or Steam Sterilization

[00887868562310]

Moist Heat or Steam Sterilization

[00887868562310]

Moist Heat or Steam Sterilization

[00887868562310]

Moist Heat or Steam Sterilization

[00887868562310]

Moist Heat or Steam Sterilization

[00887868562310]

Moist Heat or Steam Sterilization

[00887868562310]

Moist Heat or Steam Sterilization

[00887868562310]

Moist Heat or Steam Sterilization

[00887868562310]

Moist Heat or Steam Sterilization

[00887868562310]

Moist Heat or Steam Sterilization

[00887868562310]

Moist Heat or Steam Sterilization

[00887868562310]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-07-13
• Device Publish Date: 2023-07-05

On-Brand Devices [Vanguard® 360 Instrument]

• 00880304814875: 32-360842
• 00880304814868: 32-360843
• 00880304814851: 32-360841
• 00887868484780: 32-360894
• 00887868484773: 32-360893
• 00887868484766: 32-360892
• 00887868484759: 32-360891
• 00887868484742: 32-360890
• 00887868484735: 32-360889
• 00887868484728: 32-360888
• 00887868484711: 32-360887
• 00887868484704: 32-360886
• 00887868484698: 32-360885
• 00887868484681: 32-360884
• 00887868484674: 32-360883
• 00887868484667: 32-360882
• 00887868484650: 32-360881
• 00887868484391: 32-360782
• 00887868484384: 32-360780
• 00887868484377: 32-360778
• 00887868484360: 32-360776
• 00887868484353: 32-360774
• 00887868484339: 32-360770
• 00887868484322: 32-360768
• 00887868484315: 32-360766
• 00887868484308: 32-360764
• 00887868484292: 32-360762
• 00887868484285: 32-360760
• 00887868484643: 32-360840
• 00887868484636: 32-360830
• 00887868484629: 32-360828
• 00887868484612: 32-360826
• 00887868484605: 32-360824
• 00887868484599: 32-360822
• 00887868484582: 32-360820
• 00887868484575: 32-360818
• 00887868484568: 32-360816
• 00887868484551: 32-360814
• 00887868484544: 32-360812
• 00887868484537: 32-360810
• 00887868484520: 32-360808
• 00887868484513: 32-360806
• 00887868484506: 32-360804
• 00887868484490: 32-360802
• 00887868484483: 32-360800
• 00887868484476: 32-360798
• 00887868484469: 32-360796
• 00887868484452: 32-360794
• 00887868484445: 32-360792
• 00887868484438: 32-360790