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“Laborie” Biofeedback and Stimulation System - Taiwan Registration bd47c48c79a69365f50b3c7fa7fd6b31

Access comprehensive regulatory information for “Laborie” 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 bd47c48c79a69365f50b3c7fa7fd6b31 and manufactured by LABORIE MEDICAL TECHNOLOGIES CANADA ULC.. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..

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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bd47c48c79a69365f50b3c7fa7fd6b31
Registration Details
Taiwan FDA Registration: bd47c48c79a69365f50b3c7fa7fd6b31
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Device Details

“Laborie” Biofeedback and Stimulation System
TW: “雷柏瑞”生物回饋及電刺激系統
Risk Class 2
MD

Registration Details

bd47c48c79a69365f50b3c7fa7fd6b31

Ministry of Health Medical Device Import No. 025505

DHA05602550507

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology-urology devices

H5320 Non-implantable electronic urination homemade device

Imported from abroad

Dates and Status

Oct 22, 2013

Oct 22, 2023