Taiwan FDA registration a986dc43ba4a8a832686ff00366fb8f3

“Medlander” Biofeedback and Stimulation System

TW: “麥瀾德”生物回饋及電刺激系統

Taiwan·Risk Class 2·MD·Medlander Medical Technology Co., Ltd.·Registered Sep 05, 2021 – Sep 05, 2026Active

Registration details

Analysis ID: a986dc43ba4a8a832686ff00366fb8f3
License Form: Ministry of Health Medical Device Land Transport No. 001256
Customs Code: DHA09200125600

Company information

Manufacturer: Medlander Medical Technology Co., Ltd.
Manufacturer Country: China
Authorized Representative: HOYU MEDICAL CO., LTD.

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): H Gastroenterology-Urology Apparatus;; Ø Devices for physical medicine;; K Apparatus for neurology
Product Type (Level 2): O5850 Powered Muscle Stimulator;; K5050 Physiological Feedback Meter;; H5320 Non-implantable electronic urination homemade device
Import Information: Imported from abroad; Made in China

Dates and status

Registration Date: Sep 05, 2021
Expiry Date: Sep 05, 2026

About this record

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..

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