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"Schwind" Corneal Topography (Non-Sterile) - Taiwan Registration c032d46609b966a90bea30feee262eff

Access comprehensive regulatory information for "Schwind" Corneal Topography (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c032d46609b966a90bea30feee262eff and manufactured by SCHWIND EYE-TECH-SOLUTIONS GMBH. The authorized representative in Taiwan is CLINICO INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SCHWIND EYE-TECH-SOLUTIONS GMBH, and 1 recent registrations in the same category. 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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c032d46609b966a90bea30feee262eff
Registration Details
Taiwan FDA Registration: c032d46609b966a90bea30feee262eff
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Device Details

"Schwind" Corneal Topography (Non-Sterile)
TW: "่ฆ–่ฌๅพ—" ่ง’่†œๅœฐๅœ–ๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

c032d46609b966a90bea30feee262eff

Ministry of Health Medical Device Import Registration No. 021016

DHA08402101609

Company Information

Product Details

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

M Ophthalmic devices

M1350 Keatoscope

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2025

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