Taiwan FDA registration a2917787e6d6384f0ae0e9b3a4a9a49c

“i-Medical” Manual ophthalmic surgical instrument (Non-Sterile)

TW: “艾美狄克”手動式眼科手術器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·I-MEDICAL OPHTHALMIC INTERNATIONAL GMBH·Registered Jun 11, 2019 – Jun 11, 2024Expired
Registration details
Analysis ID
a2917787e6d6384f0ae0e9b3a4a9a49c
License Form
Ministry of Health Medical Device Import No. 020535
Customs Code
DHA09402053501
Company information
Manufacturer Country
Germany
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
Jun 11, 2019
Expiry Date
Jun 11, 2024
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About this record

Access comprehensive regulatory information for “i-Medical” 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 a2917787e6d6384f0ae0e9b3a4a9a49c and manufactured by I-MEDICAL OPHTHALMIC INTERNATIONAL GMBH. The authorized representative in Taiwan is Kangcheng Biomedical Technology Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including I-MEDICAL OPHTHALMIC INTERNATIONAL GMBH, 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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