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"OSCO" titanium ophthalmic equipment (unsterilized) - Taiwan Registration 9b53fc5af084ab02106f0d657814d072

Access comprehensive regulatory information for "OSCO" titanium ophthalmic 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 9b53fc5af084ab02106f0d657814d072 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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9b53fc5af084ab02106f0d657814d072
Registration Details
Taiwan FDA Registration: 9b53fc5af084ab02106f0d657814d072
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Device Details

"OSCO" titanium ophthalmic equipment (unsterilized)
TW: "ๆญๆ€็ง‘" ้ˆฆๅˆ้‡‘็œผ็ง‘ๅ™จๆ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

9b53fc5af084ab02106f0d657814d072

DHA04400142504

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

Oct 28, 2005

Oct 28, 2010

Nov 23, 2012

Cancellation Information

Logged out

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