Taiwan FDA registration 3bcb16dc0c4d214581189891f4bb6e59

"Xinbo" Medical Examination Light (Non-Sterile)

TW: "鑫博" 醫用檢查燈 (未滅菌)

Taiwan·Risk Class 1·MD·ALBERT WAESCHLE LTD.·Registered Aug 24, 2016 – Aug 24, 2021Expired

Registration details

Analysis ID: 3bcb16dc0c4d214581189891f4bb6e59
License Form: Ministry of Health Medical Device Import No. 016923
Customs Code: DHA09401692305

Company information

Manufacturer: ALBERT WAESCHLE LTD.
Manufacturer Country: United Kingdom
Authorized Representative: XIN BO ENTERPRISE 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: Aug 24, 2016
Expiry Date: Aug 24, 2021

About this record

Access comprehensive regulatory information for "Xinbo" 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 3bcb16dc0c4d214581189891f4bb6e59 and manufactured by ALBERT WAESCHLE LTD.. The authorized representative in Taiwan is XIN BO 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.