"Heidelberg" Manual Ophthalmic Surgical Instrument (Non-sterile) - Taiwan Registration 21e90360c628ee38693def5d8fbf2d0f
Access comprehensive regulatory information for "Heidelberg" 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 21e90360c628ee38693def5d8fbf2d0f and manufactured by HEIDELBERG ENGINEERING GMBH. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..
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.
Device Details
Registration Details
21e90360c628ee38693def5d8fbf2d0f
Ministry of Health Medical Device Import No. 021175
DHA09402117502
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 Ophthalmic devices
M4350 Manual Ophthalmic Surgery Instrument
Imported from abroad
Dates and Status
Jan 10, 2020
Jan 10, 2025

