MyndMove - MyndTec Inc

Duns Number:203019245

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More Product Details

Catalog Number

900167

Brand Name

MyndMove

Version/Model Number

MyndMove Electrode 5cm x 5cm

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 23, 2019

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

MR Unsafe

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K170564

Product Code Details

Product Code

GZI

Product Code Name

Stimulator, Neuromuscular, External Functional

Device Record Status

Public Device Record Key

905b17bb-a3e4-4ff9-b26f-8e989b4c2d68

Public Version Date

October 02, 2020

Public Version Number

6

DI Record Publish Date

October 24, 2017

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"MYNDTEC INC" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 51