Taiwan FDA registration 404bb1caacff3d3d3871e1af609853a1

"Schwind" Corneal Topography (Non-Sterile)

TW: "視萬得" 角膜地圖儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·SCHWIND EYE-TECH-SOLUTIONS GMBH·Registered Nov 14, 2019 – Nov 14, 2024Cancelled
Registration details
Analysis ID
404bb1caacff3d3d3871e1af609853a1
License Form
Ministry of Health Medical Device Import No. 021016
Customs Code
DHA09402101605
Company information
Manufacturer Country
Germany
Authorized Representative
CLINICO INC.
Product details
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M1350 Keatoscope
Import Information
Imported from abroad
Dates and status
Registration Date
Nov 14, 2019
Expiry Date
Nov 14, 2024
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

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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