MAXIM KNEE INSTRUMENTATION 32-379660

GUDID 05019279796472

Biomet Uk Ltd

Orthopaedic implant impactor

• Primary Device ID: 05019279796472
• NIH Device Record Key: 31d57237-9fb6-4719-8a10-b419f441c550
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MAXIM KNEE INSTRUMENTATION
• Version Model Number: 32-379660
• Catalog Number: 32-379660
• Company DUNS: 219322575
• Company Name: Biomet Uk Ltd
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	05019279796472 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[05019279796472]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-07-28

On-Brand Devices [MAXIM KNEE INSTRUMENTATION]

• 05019279796472: 32-379660
• 05019279031917: RD140513
• 05019279031900: RD140512
• 05019279467266: 32-348086
• 05019279466887: 32-348054
• 05019279465972: 32-347127