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"OSCO" AII-7000 (unsterilized) - Taiwan Registration 0553adcd6c00f54d7d8066719c2dd1fe

Access comprehensive regulatory information for "OSCO" AII-7000 (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0553adcd6c00f54d7d8066719c2dd1fe and manufactured by ASICO LLC. The authorized representative in Taiwan is WELL SHIP INDUSTRIAL 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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0553adcd6c00f54d7d8066719c2dd1fe
Registration Details
Taiwan FDA Registration: 0553adcd6c00f54d7d8066719c2dd1fe
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Device Details

"OSCO" AII-7000 (unsterilized)
TW: "ๆญๆ–ฏ็ง‘"ๆ„›ไพ-7000(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

0553adcd6c00f54d7d8066719c2dd1fe

DHA04400187904

Company Information

United States

Product Details

Manual eye surgery instruments are non-electric, hand-held devices designed to assist or perform eye surgery.

M Ophthalmology

M.4350 ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ

import

Dates and Status

Nov 11, 2005

Nov 11, 2010

Nov 23, 2012

Cancellation Information

Logged out

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