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

• 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