FDA UDI In Commercial Distribution 🇺🇸 United States

myoRESEARCH3 (MR3)

DI: 00816271020742 · Model: 405 · Noraxon U.S.A., Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
myoRESEARCH3 (MR3)
Primary DI
00816271020742
Version / Model
405
Catalog Number
405
Company Name
Noraxon U.S.A., Inc.
Labeler DUNS
611243809
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-07
Public Version
2
Public Version Date
2024-02-05
Public Version Status
Update
Public Device Record Key
37d4a2f6-6bf8-4832-bbed-8cda3742b843

Device Description

MR3 - myoMOTION

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KQX Goniometer, Ac-Powered

GMDN Terms

Code Name
47518 Biomechanical function analysis/rehabilitation software

Identifiers

Type ID
Primary 00816271020742