FDA Device Intelligence
Home › SYRMA JOHARI MEDTECH LIMITED › Johari Digital Healthcare Ltd.

Johari Digital Healthcare Ltd.

SYRMA JOHARI MEDTECH LIMITED · Model Sonicaor Plus 941 · UDI-DI 08908008085420

IMG
10
510(k) clearances
235
Adverse events (2 deaths)
2
Recalls
24
Facilities

Description

"This device is a clinical combination therapy of Ultrasound & Electrotherapy with an easy user interface and versatility to treat different body areas simultaneously. This aesthetically designed clinical model is lightweight, small in size, and is battery powered Precise treatment for pain relief Relaxation of muscle spasm Prevention of redardation of disuse atrophy Increase local blood circulation muscle re-education maintaining or increasing range of motion prevent venous thrombosis after surgery. Key Feature: • Channel : Four(941) Electrotherapy • 1 & 3 MHz Ultrasound Applicator • Large Color Touch Screen Display • Pre-programmed Protocols • Inbuilt Rechargeable Battery Pack"

Recalls

DateFirmReason
2008-02-28Chattanooga Corp IncDevice may fail to administer therapy during use.
2008-02-28Chattanooga Corp IncDevice may fail to administer therapy during use.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.