HAMMR™ 110046320

GUDID 00887868578915

Orthosoft Inc

Surgical power tool adaptor Surgical power tool adaptor Surgical power tool adaptor Surgical power tool adaptor Surgical power tool adaptor Surgical power tool adaptor Surgical power tool adaptor Surgical power tool adaptor Surgical power tool adaptor Surgical power tool adaptor Surgical power tool adaptor

• Primary Device ID: 00887868578915
• NIH Device Record Key: afcc3584-c4ab-4a7f-b0d9-99f1dfec7d46
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HAMMR™
• Version Model Number: 110046320
• Catalog Number: 110046320
• Company DUNS: 205670032
• Company Name: Orthosoft Inc
• 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(866)336-7846
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(866)336-7846
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(866)336-7846
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(866)336-7846
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(866)336-7846
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(866)336-7846
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(866)336-7846
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(866)336-7846
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(866)336-7846
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(866)336-7846
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(866)336-7846
• Email: zimmer.consumerrelations@zimmerbiomet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868578915 [Primary]

FDA Product Code

• GEY: MOTOR, SURGICAL INSTRUMENT, AC-POWERED

Sterilization

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

[00887868578915]

Moist Heat or Steam Sterilization

[00887868578915]

Moist Heat or Steam Sterilization

[00887868578915]

Moist Heat or Steam Sterilization

[00887868578915]

Moist Heat or Steam Sterilization

[00887868578915]

Moist Heat or Steam Sterilization

[00887868578915]

Moist Heat or Steam Sterilization

[00887868578915]

Moist Heat or Steam Sterilization

[00887868578915]

Moist Heat or Steam Sterilization

[00887868578915]

Moist Heat or Steam Sterilization

[00887868578915]

Moist Heat or Steam Sterilization

[00887868578915]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-05-01
• Device Publish Date: 2024-04-23

Devices Manufactured by Orthosoft Inc

• 00887868578915 - HAMMR™: 2024-05-01
• 00887868578915 - HAMMR™: 2024-05-01
• 00887868557873 - ROSA® Shoulder: 2024-03-14
• 00887868557880 - ROSA® Shoulder: 2024-03-14
• 00887868557897 - ROSA® Shoulder: 2024-03-14
• 00887868557903 - ROSA® Shoulder: 2024-03-14
• 00887868557910 - ROSA® Shoulder: 2024-03-14
• 00887868558078 - ROSA® Shoulder: 2024-03-14
• 00887868558092 - ROSA® Shoulder: 2024-03-14