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"OASIS" Manual Ophthalmic Surgical Instrument (Sterile) - Taiwan Registration 87311b2ce53e6c0c2a3a21829f92d4f2

Access comprehensive regulatory information for "OASIS" 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 87311b2ce53e6c0c2a3a21829f92d4f2 and manufactured by OASIS MEDICAL, INC.. The authorized representative in Taiwan is AMAZMED 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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87311b2ce53e6c0c2a3a21829f92d4f2
Registration Details
Taiwan FDA Registration: 87311b2ce53e6c0c2a3a21829f92d4f2
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Device Details

"OASIS" Manual Ophthalmic Surgical Instrument (Sterile)
TW: "็ถ ๆดฒ"ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ(ๆป…่Œ)
Risk Class 1
MD

Registration Details

87311b2ce53e6c0c2a3a21829f92d4f2

Ministry of Health Medical Device Import No. 018670

DHA09401867002

Company Information

United States

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

Dec 29, 2017

Dec 29, 2022