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"Optikon" Manual ophthalmic surgical instrument (Sterile) - Taiwan Registration 3380fbb0813bfdc43b37f0f6c043e67c

Access comprehensive regulatory information for "Optikon" Manual ophthalmic surgical instrument (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3380fbb0813bfdc43b37f0f6c043e67c and manufactured by OPTIKON 2000 S. P. A. The authorized representative in Taiwan is CLINICO INC..

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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3380fbb0813bfdc43b37f0f6c043e67c
Registration Details
Taiwan FDA Registration: 3380fbb0813bfdc43b37f0f6c043e67c
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Device Details

"Optikon" Manual ophthalmic surgical instrument (Sterile)
TW: "ๅฅงๅบท" ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ (ๆป…่Œ)
Risk Class 1
MD

Registration Details

3380fbb0813bfdc43b37f0f6c043e67c

Ministry of Health Medical Device Import No. 019247

DHA09401924706

Company Information

Italy

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".

M Ophthalmic devices

M4350 Manual Ophthalmic Surgery Instrument

Imported from abroad

Dates and Status

Jun 28, 2018

Jun 28, 2028