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"Siji" manual eye surgery instruments (sterilization) - Taiwan Registration 58c4586a51ce13814fb8938d0cbd345f

Access comprehensive regulatory information for "Siji" manual eye surgery instruments (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 58c4586a51ce13814fb8938d0cbd345f and manufactured by SURGICAL SPECIALTIES CORPORATION. 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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58c4586a51ce13814fb8938d0cbd345f
Registration Details
Taiwan FDA Registration: 58c4586a51ce13814fb8938d0cbd345f
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Device Details

"Siji" manual eye surgery instruments (sterilization)
TW: โ€œๆ€ๅ‰โ€ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ๏ผˆๆป…่Œ๏ผ‰
Risk Class 1
Cancelled

Registration Details

58c4586a51ce13814fb8938d0cbd345f

DHA04400817605

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

Oct 02, 2009

Oct 02, 2019

Aug 05, 2022

Cancellation Information

Logged out

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