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“Medikit” Supercath C-Pro - Taiwan Registration 87fbc22ac9385993c2465e4863e4f1bf

Access comprehensive regulatory information for “Medikit” Supercath C-Pro in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 87fbc22ac9385993c2465e4863e4f1bf and manufactured by TOGO MEDIKIT CO., LTD. HYUGA FACTORY. The authorized representative in Taiwan is EVERMEDICAL COMPANY 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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87fbc22ac9385993c2465e4863e4f1bf
Registration Details
Taiwan FDA Registration: 87fbc22ac9385993c2465e4863e4f1bf
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Device Details

“Medikit” Supercath C-Pro
TW: “美迪克”安全血液透析血管留置針
Risk Class 2
MD

Registration Details

87fbc22ac9385993c2465e4863e4f1bf

Ministry of Health Medical Device Import No. 032673

DHA05603267306

Company Information

Product Details

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

H Gastroenterology-urology devices

H5540 Blood access devices and accessories

Imported from abroad

Dates and Status

May 24, 2019

May 24, 2024