FDA UDI Not in Commercial Distribution 🇺🇸 United States

MJS System 3 Upgrade

DI: 00718175004067 · Model: 850-822 · BIODEX MEDICAL SYSTEMS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MJS System 3 Upgrade
Primary DI
00718175004067
Version / Model
850-822
Catalog Number
850-822
Company Name
BIODEX MEDICAL SYSTEMS, INC.
Labeler DUNS
043833813
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-10
Public Version
3
Public Version Date
2023-07-25
Public Version Status
Update
Public Device Record Key
deb0798e-a553-4ce1-bfca-fe95a41e838a
Distribution End Date
2023-07-24

Device Description

Biodex Multi-Joint-System 3 Rev.1 UpGrade

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IKK System, Isokinetic Testing And Evaluation

GMDN Terms

Code Name
63457 Biomechanical function analysis system, force-testing, stationary

Identifiers

Type ID
Primary 00718175004067