FDA UDI Not in Commercial Distribution 🇺🇸 United States

Kintinuum™

DI: B493SW0042 · Model: SW-0042 · MC10, INC.
Product Codes
1
GMDN Terms
3
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Kintinuum™
Primary DI
B493SW0042
Version / Model
SW-0042
Company Name
MC10, INC.
Labeler DUNS
829221139
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-02-01
Public Version
4
Public Version Date
2024-02-05
Public Version Status
Update
Public Device Record Key
a76ee68b-6b92-40e3-b075-4f248870f7cd
Distribution End Date
2021-04-01

Device Description

Patient application for Android

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
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
ISD Exerciser, Measuring

GMDN Terms

Code Name
33652 Electronic goniometer/kinesiology sensor
36252 Kinesiology ambulatory recorder
47518 Biomechanical function analysis/rehabilitation software

Identifiers

Type ID
Primary B493SW0042

Customer Contacts

Phone
8572145630