Taiwan FDA registration 9a5d1758372fcd4d18e9c96210cbbf97

"ASICO" Manual Ophthalmic Surgical Instrument (Non-Sterile)

TW: "艾思可" 手動式眼科手術器械(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·ASICO LLC·Registered May 13, 2019 – May 13, 2024Expired
Registration details
Analysis ID
9a5d1758372fcd4d18e9c96210cbbf97
License Form
Ministry of Health Medical Device Import No. 020443
Customs Code
DHA09402044306
Company information
Manufacturer
ASICO LLC
Manufacturer Country
United States
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M4350 Manual Ophthalmic Surgery Instrument
Import Information
Imported from abroad
Dates and status
Registration Date
May 13, 2019
Expiry Date
May 13, 2024
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About this record

Access comprehensive regulatory information for "ASICO" Manual Ophthalmic Surgical Instrument (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9a5d1758372fcd4d18e9c96210cbbf97 and manufactured by ASICO LLC. The authorized representative in Taiwan is UNIVERSAL VISION BIOTECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ASICO LLC, and 1 recent registrations in the same category. 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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