HAMMR™ 110049103

GUDID 00889024663824

Biomet Orthopedics, LLC

Surgical power tool adaptor

• Primary Device ID: 00889024663824
• NIH Device Record Key: f413f6f4-2016-4ceb-8df3-9307989c3867
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HAMMR™
• Version Model Number: 110049103
• Catalog Number: 110049103
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024663824 [Primary]

FDA Product Code

• GEY: MOTOR, SURGICAL INSTRUMENT, AC-POWERED

Sterilization

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

[00889024663824]

Moist Heat or Steam Sterilization

[00889024663824]

Moist Heat or Steam Sterilization

[00889024663824]

Moist Heat or Steam Sterilization

[00889024663824]

Moist Heat or Steam Sterilization

[00889024663824]

Moist Heat or Steam Sterilization

[00889024663824]

Moist Heat or Steam Sterilization

[00889024663824]

Moist Heat or Steam Sterilization

[00889024663824]

Moist Heat or Steam Sterilization

[00889024663824]

Moist Heat or Steam Sterilization

[00889024663824]

Moist Heat or Steam Sterilization

[00889024663824]

Moist Heat or Steam Sterilization

[00889024663824]

Moist Heat or Steam Sterilization

[00889024663824]

Moist Heat or Steam Sterilization

[00889024663824]

Moist Heat or Steam Sterilization

[00889024663824]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-05-17
• Device Publish Date: 2024-05-09

On-Brand Devices [HAMMR™]

• 00889024663862: 110049107
• 00889024663855: 110049106
• 00889024663848: 110049105
• 00889024663831: 110049104
• 00889024663824: 110049103
• 00889024663817: 110049102
• 00889024663800: 110049101
• 00889024663794: 110049100
• 00889024674288: 110049108