Taiwan FDA registration f05dd47372fb28a3b3af38153d1f1fc9

"HEINE" Medical Examination Light (Non-Sterile)

TW: "海尼恩" 醫用檢查燈 (未滅菌)

Taiwan·Risk Class 1·MD·HEINE OPTOTECHNIK GMBH & CO. KG·Registered Jan 15, 2014 – Jan 15, 2024Expired

Registration details

Analysis ID: f05dd47372fb28a3b3af38153d1f1fc9
License Form: Ministry of Health Medical Device Import No. 013781
Customs Code: DHA09401378109

Company information

Manufacturer: HEINE OPTOTECHNIK GMBH & CO. KG
Manufacturer Country: Germany
Authorized Representative: DENSO SCIENTIFIC CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Light Source for Optical Fiber Dentistry (F.4620)".
Product Type (Level 1): F Dental devices
Product Type (Level 2): F4620 Light source for photofiber dentistry
Import Information: Imported from abroad

Dates and status

Registration Date: Jan 15, 2014
Expiry Date: Jan 15, 2024

About this record

Access comprehensive regulatory information for "HEINE" Medical Examination Light (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 f05dd47372fb28a3b3af38153d1f1fc9 and manufactured by HEINE OPTOTECHNIK GMBH & CO. KG. The authorized representative in Taiwan is DENSO SCIENTIFIC CO., LTD..

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