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"Esco" manual eye surgery instruments (unsterilized) - Taiwan Registration 85e90adbf8e374e7fc045d197baf1736

Access comprehensive regulatory information for "Esco" manual eye surgery instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 85e90adbf8e374e7fc045d197baf1736 and manufactured by ASICO LLC. The authorized representative in Taiwan is ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND).

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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85e90adbf8e374e7fc045d197baf1736
Registration Details
Taiwan FDA Registration: 85e90adbf8e374e7fc045d197baf1736
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Device Details

"Esco" manual eye surgery instruments (unsterilized)
TW: โ€œๆ„›ๆ–ฏๅฏโ€ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

85e90adbf8e374e7fc045d197baf1736

DHA04400634301

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

import

Dates and Status

Nov 30, 2007

Nov 30, 2022

Apr 12, 2024

Cancellation Information

Logged out

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