e-vive NMES System; Large/XL, Left - e-vive NMES System; Large/XL, Left - CYMEDICA ORTHOPEDICS, INC.

Duns Number:035596579

Device Description: e-vive NMES System; Large/XL, Left

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More Product Details

Catalog Number

CY-1000-017

Brand Name

e-vive NMES System; Large/XL, Left

Version/Model Number

CY-1000-017

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

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"

Yes

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

K163067

Product Code Details

Product Code

GZJ

Product Code Name

Stimulator, Nerve, Transcutaneous, For Pain Relief

Device Record Status

Public Device Record Key

29c41632-0756-40f8-a8c3-57b5cd412f03

Public Version Date

February 19, 2021

Public Version Number

7

DI Record Publish Date

February 08, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"CYMEDICA ORTHOPEDICS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 90
2 A medical device with a moderate to high risk that requires special controls. 91