Taiwan FDA registration f2d7626451a9a9204fa3411e3c7faf52

"Kunlin" intraoral camera (unsterilized)

TW: “昆霖”口內攝影機 (未滅菌)

Taiwan·Risk Class 1·QUEN LIN INSTRUMENTS CO., LTD.·Registered Aug 16, 2006 – Aug 16, 2026Active

Registration details

Analysis ID: f2d7626451a9a9204fa3411e3c7faf52

Company information

Manufacturer: QUEN LIN INSTRUMENTS CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: QUEN LIN INSTRUMENTS CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Classification and Grading of Medical Devices "Surgical Cameras and Their Accessories (I.4160)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4160 Surgical cameras and accessories thereof
Import Information: Domestic

Dates and status

Registration Date: Aug 16, 2006
Expiry Date: Aug 16, 2026

About this record

Access comprehensive regulatory information for "Kunlin" intraoral camera (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f2d7626451a9a9204fa3411e3c7faf52 and manufactured by QUEN LIN INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is QUEN LIN INSTRUMENTS CO., LTD..

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