Pure Global

"Puotis" keratoscope (unsterilized) - Taiwan Registration d5f10eb7d54f2edb9b2304ff56de7c13

Access comprehensive regulatory information for "Puotis" keratoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d5f10eb7d54f2edb9b2304ff56de7c13 and manufactured by PLUSOPTIX GMBH. The authorized representative in Taiwan is EVERVISION INSTRUMENT CO..

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
d5f10eb7d54f2edb9b2304ff56de7c13
Registration Details
Taiwan FDA Registration: d5f10eb7d54f2edb9b2304ff56de7c13
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Puotis" keratoscope (unsterilized)
TW: โ€œๆ™ฎๅฅงๆๆ–ฏโ€่ง’่†œ้ก(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

d5f10eb7d54f2edb9b2304ff56de7c13

DHA04401220501

Company Information

Germany

Product Details

Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.

M Ophthalmology

M.1350 Coratoscope

import

Dates and Status

Sep 26, 2012

Sep 26, 2017

Dec 13, 2019

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ