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"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.

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21e90360c628ee38693def5d8fbf2d0f
Registration Details
Taiwan FDA Registration: 21e90360c628ee38693def5d8fbf2d0f
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Device Details

"Heidelberg" Manual Ophthalmic Surgical Instrument (Non-sterile)
TW: "ๆตทๅพทๅ ก"ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

21e90360c628ee38693def5d8fbf2d0f

Ministry of Health Medical Device Import No. 021175

DHA09402117502

Company Information

Germany

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