Pure Global

Taisho and autoclaves - Taiwan Registration 5cf50f3206ded2f4eed3862b0ccad694

Access comprehensive regulatory information for Taisho and autoclaves in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5cf50f3206ded2f4eed3862b0ccad694 and manufactured by TA CHENG HO INSTRUMENT CO., LTD.. The authorized representative in Taiwan is TA CHENG HO INSTRUMENT 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
5cf50f3206ded2f4eed3862b0ccad694
Registration Details
Taiwan FDA Registration: 5cf50f3206ded2f4eed3862b0ccad694
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Taisho and autoclaves
TW: ๅคงๆญฃๅ’Œ้ซ˜ๅฃ“่’ธๆฐฃๆป…่Œๅ™จ
Risk Class 2

Registration Details

5cf50f3206ded2f4eed3862b0ccad694

DHY00500362600

Company Information

Taiwan, Province of China

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

Domestic

Dates and Status

Mar 23, 2012

Mar 23, 2027