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Neuro Touch

FDA UDI

Class I (US FDA UDI)

by Yostra Labs Private Limited

Identity

Trade Name
NEURO TOUCH FDA UDI
Generic Name
Vibratory biothesiometer FDA UDI
Device Name
NEURO TOUCH is a point of care screening device for Peripheral Neuropathy. Perform the following tests using NEURO TOUCH: Protective Sensation Test (Monofilament Test) Vibration Perception Test Hot and Cold Perception Test. FDA UDI
Model / Reference
SDNTST0123US FDA UDI
Description
NEURO TOUCH is a point of care screening device for Peripheral Neuropathy. Perform the following tests using NEURO TOUCH: Protective Sensation Test (Monofilament Test) Vibration Perception Test Hot and Cold Perception Test. FDA UDI

Identifiers

Primary DI / UDI-DI
08908022363016 FDA UDI
FDA Product Code
GXB FDA UDI
LLN FDA UDI
LQW FDA UDI
GMDN Term
Vibratory biothesiometer FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.1500 FDA UDI
882.1200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Thermotester, diagnosticVibratory biothesiometerPressure algometer/aesthesiometer, electronic

Neuro Touch by Yostra Labs Private Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pressure algometer/aesthesiometer, electronic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5350e077-3332-4e74-9861-bb73e6bb6d14 34 fields · synced Jun 1, 2026