Taiwan FDA registration dcfd9c6222e6944fb43603171bf41e42

"Riverpoint" Operating headlamp (Non-Sterile)

TW: "瑞浦特" 手術用頭燈 (未滅菌)

Taiwan·Risk Class 1·MD·RIVERPOINT MEDICAL·Registered Dec 30, 2016 – Dec 30, 2026Active

Registration details

Analysis ID: dcfd9c6222e6944fb43603171bf41e42
License Form: Ministry of Health Medical Device Import No. 017348
Customs Code: DHA09401734802

Company information

Manufacturer: RIVERPOINT MEDICAL
Manufacturer Country: United States
Authorized Representative: MENEY CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Surgical Headlamps (M.4335)".
Product Type (Level 1): M Ophthalmic devices
Product Type (Level 2): M4335 Surgical headlamp
Import Information: Imported from abroad

Dates and status

Registration Date: Dec 30, 2016
Expiry Date: Dec 30, 2026

About this record

Access comprehensive regulatory information for "Riverpoint" Operating headlamp (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 dcfd9c6222e6944fb43603171bf41e42 and manufactured by RIVERPOINT MEDICAL. The authorized representative in Taiwan is MENEY CO., LTD..

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