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Johari Digital Healthcare Limited

FDA UDI

Class II (US FDA UDI)

by Syrma Johari Medtech Limited

Identity

Trade Name
Johari Digital Healthcare Limited FDA UDI
Generic Name
Physical therapy ultrasound/neuromuscular stimulation system FDA UDI
Model / Reference
WS2U-Combo Device FDA UDI

Identifiers

Primary DI / UDI-DI
08908008085017 FDA UDI
FDA Product Code
IMG FDA UDI
GMDN Term
Physical therapy ultrasound/neuromuscular stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5860 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Physical therapy ultrasound/neuromuscular stimulation system

Johari Digital Healthcare Limited by Syrma Johari Medtech Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Physical therapy ultrasound/neuromuscular stimulation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5cde2806-6893-4d3a-89b8-5e16ca8e26bc 32 fields · synced May 31, 2026