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“Medlander” Biofeedback and Stimulation System - Taiwan Registration a986dc43ba4a8a832686ff00366fb8f3

Access comprehensive regulatory information for “Medlander” Biofeedback and Stimulation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a986dc43ba4a8a832686ff00366fb8f3 and manufactured by Medlander Medical Technology Co., Ltd.. The authorized representative in Taiwan is HOYU MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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a986dc43ba4a8a832686ff00366fb8f3
Registration Details
Taiwan FDA Registration: a986dc43ba4a8a832686ff00366fb8f3
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Device Details

“Medlander” Biofeedback and Stimulation System
TW: “麥瀾德”生物回饋及電刺激系統
Risk Class 2
MD

Registration Details

a986dc43ba4a8a832686ff00366fb8f3

Ministry of Health Medical Device Land Transport No. 001256

DHA09200125600

Company Information

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology-Urology Apparatus;; Ø Devices for physical medicine;; K Apparatus for neurology

O5850 Powered Muscle Stimulator;; K5050 Physiological Feedback Meter;; H5320 Non-implantable electronic urination homemade device

Imported from abroad; Made in China

Dates and Status

Sep 05, 2021

Sep 05, 2026