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"Bivier" Manual Eye Surgery Instruments (Sterilized) - Taiwan Registration d97bd667eeec751f97e5317f856be0ad

Access comprehensive regulatory information for "Bivier" Manual Eye Surgery Instruments (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d97bd667eeec751f97e5317f856be0ad and manufactured by BEAVER-VISITEC INTERNATIONAL, INC.. 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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d97bd667eeec751f97e5317f856be0ad
Registration Details
Taiwan FDA Registration: d97bd667eeec751f97e5317f856be0ad
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Device Details

"Bivier" Manual Eye Surgery Instruments (Sterilized)
TW: "็•ขๅจ่‰พ" ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

d97bd667eeec751f97e5317f856be0ad

DHA09401752501

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 Ophthalmology

M.4350 ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ

Input;; QMS/QSD

Dates and Status

Feb 24, 2017

Feb 24, 2022

Apr 12, 2024

Cancellation Information

Logged out

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