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"Jeli" manual instruments for general surgery (unsterilized) - Taiwan Registration e29af16757f03c03201636d67a81a95e

Access comprehensive regulatory information for "Jeli" manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e29af16757f03c03201636d67a81a95e and manufactured by JEIL TECH CO., LTD.. The authorized representative in Taiwan is LA MED INTERNATIONAL 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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e29af16757f03c03201636d67a81a95e
Registration Details
Taiwan FDA Registration: e29af16757f03c03201636d67a81a95e
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Device Details

"Jeli" manual instruments for general surgery (unsterilized)
TW: โ€œๅ‚‘็ซ‹โ€ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

e29af16757f03c03201636d67a81a95e

DHA04401319707

Company Information

Korea, Republic of

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".

I General, Plastic Surgery and Dermatology

I.4800 Hand Instruments for General Surgery

import

Dates and Status

Jul 10, 2013

Jul 10, 2018

Aug 18, 2015

Cancellation Information

Logged out

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