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"Jetti" casing - Taiwan Registration c882d6f2808eed70e089a5e7f22568d7

Access comprehensive regulatory information for "Jetti" casing in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c882d6f2808eed70e089a5e7f22568d7 and manufactured by JEIL TECH CO., LTD.. The authorized representative in Taiwan is CHENG ANN TECHNOLOGY 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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c882d6f2808eed70e089a5e7f22568d7
Registration Details
Taiwan FDA Registration: c882d6f2808eed70e089a5e7f22568d7
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Device Details

"Jetti" casing
TW: โ€œๆท่’‚โ€ๅฅ—็ฎก
Risk Class 2

Registration Details

c882d6f2808eed70e089a5e7f22568d7

DHA05602712902

Company Information

Korea, Republic of

Product Details

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

J General hospital and personal use equipment

J.5570 Subcutaneous single-chamber needle

import

Dates and Status

Mar 09, 2015

Mar 09, 2030