BioMotion® Cannulated 1st MPJ Hemi System HM 3010

GUDID M269HM30101

Integra® BioMotion® Cannulated Hemi System The slide hammer is used to assist with implant placement into the bone.

Ascension Orthopedics, Inc.

Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable

• Primary Device ID: M269HM30101
• NIH Device Record Key: 435d0549-b206-4ed6-bdf4-7e76bf936783
• Commercial Distribution Discontinuation: 2026-12-31
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BioMotion® Cannulated 1st MPJ Hemi System
• Version Model Number: HM 3010
• Catalog Number: HM 3010
• Company DUNS: 942377524
• Company Name: Ascension Orthopedics, 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(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.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	10381780245513 [Primary]
HIBCC	M269HM30101 [Secondary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[M269HM30101]

Moist Heat or Steam Sterilization

[M269HM30101]

Moist Heat or Steam Sterilization

[M269HM30101]

Moist Heat or Steam Sterilization

[M269HM30101]

Moist Heat or Steam Sterilization

[M269HM30101]

Moist Heat or Steam Sterilization

[M269HM30101]

Moist Heat or Steam Sterilization

[M269HM30101]

Moist Heat or Steam Sterilization

[M269HM30101]

Moist Heat or Steam Sterilization

[M269HM30101]

Moist Heat or Steam Sterilization

[M269HM30101]

Moist Heat or Steam Sterilization

[M269HM30101]

Moist Heat or Steam Sterilization

[M269HM30101]

Moist Heat or Steam Sterilization

[M269HM30101]

Moist Heat or Steam Sterilization

[M269HM30101]

Moist Heat or Steam Sterilization

[M269HM30101]

Moist Heat or Steam Sterilization

[M269HM30101]

Moist Heat or Steam Sterilization

[M269HM30101]

Moist Heat or Steam Sterilization

[M269HM30101]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2023-02-22
• Device Publish Date: 2017-09-05

On-Brand Devices [BioMotion® Cannulated 1st MPJ Hemi System]

• M269HM7000L1: Integra® BioMotion® Cannulated Hemi System The BioMotion Lid is the top part of the hemi steri
• M269HM70001: Integra® BioMotion® Cannulated Hemi System The BioMotion Hemi Sterilization Tray is designed t
• M269HM30301: Integra® BioMotion® Cannulated Hemi System The BioMotion hemi rasp is a coarse file to remove
• M269HM30101: Integra® BioMotion® Cannulated Hemi System The slide hammer is used to assist with implant pla
• M269HW11001: Integra® BioMotion® Cannulated Hemi System The smooth guide wire is used as a guide for placem