BioMotion® Cannulated 1st MPJ Hemi System HM 3030
GUDID M269HM30301
Integra® BioMotion® Cannulated Hemi System The BioMotion hemi rasp is a coarse file to remove bone.
Ascension Orthopedics, Inc.
Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable| Primary Device ID | M269HM30301 |
| NIH Device Record Key | 0ab91fd9-34c7-49c4-868a-d779166f6e1d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BioMotion® Cannulated 1st MPJ Hemi System |
| Version Model Number | HM 3030 |
| Catalog Number | HM 3030 |
| 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 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| 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 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 | 10381780245520 [Primary] |
| HIBCC | M269HM30301 [Secondary] |
FDA Product Code
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
[M269HM30301]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2022-06-10 |
| 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 |
Trademark Results [BioMotion]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 BIOMOTION 77827212 not registered Dead/Abandoned |
Applied Technology Holdings, Inc. 2009-09-15 |
 BIOMOTION 77662183 3926200 Live/Registered |
ASCENSION ORTHOPEDICS, INC. 2009-02-03 |
 BIOMOTION 77583125 3657031 Dead/Cancelled |
ZUMTOBEL LIGHTING GMBH 2008-10-01 |
 BIOMOTION 74033751 not registered Dead/Abandoned |
Biomotion Foundation, The 1990-03-01 |
 BIOMOTION 73752907 1625822 Dead/Cancelled |
SUTTER BIOMEDICAL INC. 1988-09-19 |
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