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"Schwind" Corneal Topography (Non-Sterile) - Taiwan Registration 404bb1caacff3d3d3871e1af609853a1

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 404bb1caacff3d3d3871e1af609853a1 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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404bb1caacff3d3d3871e1af609853a1
Registration Details
Taiwan FDA Registration: 404bb1caacff3d3d3871e1af609853a1
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Device Details

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

Registration Details

404bb1caacff3d3d3871e1af609853a1

Ministry of Health Medical Device Import No. 021016

DHA09402101605

Company Information

Product Details

M Ophthalmic devices

M1350 Keatoscope

Imported from abroad

Dates and Status

Nov 14, 2019

Nov 14, 2024

Cancellation Information

Logged out

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