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"Alcon" Ruida limb equipment (unsterilized) - Taiwan Registration 4c8cf6ed5e7532dafe995cbf783be8d3

Access comprehensive regulatory information for "Alcon" Ruida limb equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4c8cf6ed5e7532dafe995cbf783be8d3 and manufactured by ALCARE CO., LTD., CHIBA FACTORY WEST. The authorized representative in Taiwan is HORIZON INSTRUMENTS 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.

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4c8cf6ed5e7532dafe995cbf783be8d3
Registration Details
Taiwan FDA Registration: 4c8cf6ed5e7532dafe995cbf783be8d3
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Device Details

"Alcon" Ruida limb equipment (unsterilized)
TW: โ€œๆ„›ๆจ‚ๅบทโ€็‘ž้”่‚ข้ซ”่ฃๅ…ท๏ผˆๆœชๆป…่Œ๏ผ‰
Risk Class 1
Cancelled

Registration Details

4c8cf6ed5e7532dafe995cbf783be8d3

DHA04400569909

Company Information

Product Details

Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.

o Physical Medical Sciences

O.3475 Limb fittings

import

Dates and Status

Mar 26, 2007

Mar 26, 2022

Sep 30, 2021

Cancellation Information

Logged out

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