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NeuroSolutions 100

FDA UDI

Class II (US FDA UDI)

by Dyansys India Private Limited

Identity

Trade Name
NeuroSolutions 100 FDA UDI
Generic Name
Acupuncture electrical stimulation system FDA UDI
Device Name
NeuroSolutions 100 FDA UDI
Model / Reference
NeuroSolutions 100 FDA UDI
Description
NeuroSolutions 100 FDA UDI

Identifiers

Primary DI / UDI-DI
08908006064090 FDA UDI
FDA Product Code
NHI FDA UDI
GMDN Term
Acupuncture electrical stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5890 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Acupuncture electrical stimulation system

NeuroSolutions 100 by Dyansys India Private Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Acupuncture electrical stimulation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3196100b-85ba-42e0-8a5c-e27989319dc4 33 fields · synced May 30, 2026