Taiwan FDA registration 21e90360c628ee38693def5d8fbf2d0f

"Heidelberg" Manual Ophthalmic Surgical Instrument (Non-sterile)

TW: "海德堡"手動式眼科手術器械 (未滅菌)

Taiwan·Risk Class 1·MD·HEIDELBERG ENGINEERING GMBH·Registered Jan 10, 2020 – Jan 10, 2025Expired

Registration details

Analysis ID: 21e90360c628ee38693def5d8fbf2d0f
License Form: Ministry of Health Medical Device Import No. 021175
Customs Code: DHA09402117502

Company information

Manufacturer: HEIDELBERG ENGINEERING GMBH
Manufacturer Country: Germany
Authorized Representative: TAIWAN HWA IN ENTERPRISE 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 Ophthalmic devices
Product Type (Level 2): M4350 Manual Ophthalmic Surgery Instrument
Import Information: Imported from abroad

Dates and status

Registration Date: Jan 10, 2020
Expiry Date: Jan 10, 2025

About this record

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..

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