Pure Global

CapitaLand steam sterilizer - Taiwan Registration aa815e78cee83d18c5fe4dbecad05a3e

Access comprehensive regulatory information for CapitaLand steam sterilizer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aa815e78cee83d18c5fe4dbecad05a3e and manufactured by ZHEJIANG GETIDY MEDICAL INSTRUMENT CO., LTD.. The authorized representative in Taiwan is KAO TECH MD 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
aa815e78cee83d18c5fe4dbecad05a3e
Registration Details
Taiwan FDA Registration: aa815e78cee83d18c5fe4dbecad05a3e
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

CapitaLand steam sterilizer
TW: โ€œๅ‡ฑๅพท้†ซ็™‚โ€่’ธๆฐฃๆป…่Œๅ™จ
Risk Class 2

Registration Details

aa815e78cee83d18c5fe4dbecad05a3e

DHA09200115109

Company Information

Product Details

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

J General hospital and personal use equipment

J.6880 Sterilizer for steam

Chinese goods;; input

Dates and Status

Mar 30, 2020

Mar 30, 2030