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e-vive NMES System

FDA UDI

Class I (US FDA UDI)

by Motive Health, Inc.

Identity

Trade Name
e-vive NMES System FDA UDI
Generic Name
Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI
Device Name
e-vive Bilateral NMES System; Small / Medium FDA UDI
Model / Reference
CY-1000-051 FDA UDI
Description
e-vive Bilateral NMES System; Small / Medium FDA UDI

Identifiers

Catalog Number
CY-1000-051 FDA UDI
Primary DI / UDI-DI
00854691008087 FDA UDI
510(k) Number
K163067 FDA UDI
FDA Product Code
KQX FDA UDI
GZJ FDA UDI
IPF FDA UDI
GMDN Term
Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1500 FDA UDI
882.5890 FDA UDI
890.5850 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 16 Inch FDA UDI

Category: Physical therapy transcutaneous neuromuscular electrical stimulation system

e-vive NMES System by Motive Health, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Physical therapy transcutaneous neuromuscular electrical stimulation system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Motive Health, Inc.

Sources (1)

  • FDA UDI 118a0434-014e-4621-9a3f-cb68b8ab95d3 38 fields · synced Jun 1, 2026