Vanguard® Instrument 32-360588

GUDID 00887868563683

Biomet Orthopedics, LLC

Knee tibia prosthesis trial, reusable

• Primary Device ID: 00887868563683
• NIH Device Record Key: 361b10cf-1996-430a-b718-89fc5ea54885
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vanguard® Instrument
• Version Model Number: 32-360588
• Catalog Number: 32-360588
• 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	00887868563683 [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

[00887868563683]

Moist Heat or Steam Sterilization

[00887868563683]

Moist Heat or Steam Sterilization

[00887868563683]

Moist Heat or Steam Sterilization

[00887868563683]

Moist Heat or Steam Sterilization

[00887868563683]

Moist Heat or Steam Sterilization

[00887868563683]

Moist Heat or Steam Sterilization

[00887868563683]

Moist Heat or Steam Sterilization

[00887868563683]

Moist Heat or Steam Sterilization

[00887868563683]

Moist Heat or Steam Sterilization

[00887868563683]

Moist Heat or Steam Sterilization

[00887868563683]

Moist Heat or Steam Sterilization

[00887868563683]

Moist Heat or Steam Sterilization

[00887868563683]

Moist Heat or Steam Sterilization

[00887868563683]

Moist Heat or Steam Sterilization

[00887868563683]

Moist Heat or Steam Sterilization

[00887868563683]

Moist Heat or Steam Sterilization

[00887868563683]

Moist Heat or Steam Sterilization

[00887868563683]

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® Instrument]

• 00887868494772: 32-486261
• 00887868495151: 32-486816
• 00887868495137: 32-486806
• 00887868495113: 32-486804
• 00887868494642: 32-486204
• 00887868494598: 32-486131
• 00887868494185: 32-485262
• 00887868494178: 32-485261
• 00887868494161: 32-485260
• 00887868494130: 32-485214
• 00887868494123: 32-485210
• 00887868484797: 32-360900
• 00887868494192: 32-485263
• 00887868494833: 32-486510
• 70880304349994: 32-486255
• 00887868494666: 32-486209
• 00887868494673: 32-486210
• 00887868494635: 32-486202
• 00887868494628: 32-486201
• 00887868494604: 32-486135
• 00887868494581: 32-486130
• 00887868496677: 32-488057
• 00887868496653: 32-488055
• 00887868496639: 32-488053
• 00887868496615: 32-488051
• 70887868494726: 32-486254
• 00887868563713: 32-360594
• 00887868563706: 32-360592
• 00887868563690: 32-360590
• 00887868563683: 32-360588
• 00887868563676: 32-360586
• 00887868563669: 32-360584
• 00887868563652: 32-360582
• 00887868563645: 32-360580
• 00887868563638: 32-360574
• 00887868563621: 32-360572
• 00887868563614: 32-360570
• 00887868563607: 32-360568
• 00887868563591: 32-360566
• 00887868563584: 32-360564
• 00887868563577: 32-360562
• 00887868563560: 32-360560
• 00887868563553: 32-360554
• 00887868563546: 32-360552
• 00887868563539: 32-360550
• 00887868563522: 32-360548
• 00887868563515: 32-360546
• 00887868563508: 32-360544
• 00887868563492: 32-360542
• 00887868563485: 32-360540