Taiwan FDA registration eab54563631bf472284dc7e452e81597

"Io" Manual Eye Surgery Instruments (Unsterilized)

TW: “愛歐”手動式眼科手術器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·AMERICAN OPTISURGICAL INC.·Registered Aug 08, 2006 – Aug 08, 2011Cancelled
Registration details
Analysis ID
eab54563631bf472284dc7e452e81597
Customs Code
DHA04400503205
Company information
Manufacturer Country
United States
Authorized Representative
EVERLIGHT INSTRUMENT CO., LTD.
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 Ophthalmology
Product Type (Level 2)
M.4350 手動式眼科手術器械
Import Information
import
Dates and status
Registration Date
Aug 08, 2006
Expiry Date
Aug 08, 2011
Cancellation Date
Oct 26, 2012
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Io" 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 eab54563631bf472284dc7e452e81597 and manufactured by AMERICAN OPTISURGICAL INC.. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including AMERICAN OPTISURGICAL INC., and 2 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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