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"Tin Lok" Hult analysis software - Taiwan Registration a05c05ffdb608db78266b9fb7a6dd4f1

Access comprehensive regulatory information for "Tin Lok" Hult analysis software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a05c05ffdb608db78266b9fb7a6dd4f1 and manufactured by SCHILLER AG. The authorized representative in Taiwan is FUTUREMED TECHNOLOGY CORPORATION.

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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a05c05ffdb608db78266b9fb7a6dd4f1
Registration Details
Taiwan FDA Registration: a05c05ffdb608db78266b9fb7a6dd4f1
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Device Details

"Tin Lok" Hult analysis software
TW: โ€œ้Œซๆจ‚โ€้œ็‰นๅผๅˆ†ๆž่ปŸ้ซ”
Risk Class 2
Cancelled

Registration Details

a05c05ffdb608db78266b9fb7a6dd4f1

DHA05602929809

Company Information

Switzerland

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

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import

Dates and Status

Feb 06, 2017

Feb 06, 2022

Apr 12, 2024

Cancellation Information

Logged out

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