Taiwan FDA registration 3991204f2d3402d6845f4a8188b8484a

"Ruibang" optical fiber dental light source (unsterilized) 

TW: "瑞邦" 光纖維牙科用光源 (未滅菌) 
Taiwan flagTaiwan·Risk Class 1·RAYBOW GMBH·Registered Apr 01, 2011 – Apr 01, 2016Cancelled
Registration details
Analysis ID
3991204f2d3402d6845f4a8188b8484a
Customs Code
DHA04401012901
Company information
Manufacturer
RAYBOW GMBH
Manufacturer Country
Germany
Authorized Representative
KUO HWA DENTAL SUPPLIERS 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 Dentistry
Product Type (Level 2)
F.4620 Light source for optical fiber dentistry
Import Information
import
Dates and status
Registration Date
Apr 01, 2011
Expiry Date
Apr 01, 2016
Cancellation Date
May 21, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Ruibang" optical fiber dental light source (unsterilized)  in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3991204f2d3402d6845f4a8188b8484a and manufactured by RAYBOW GMBH. The authorized representative in Taiwan is KUO HWA DENTAL SUPPLIERS 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.

Free DatabasePowered by Pure Global AI89,000+ Devices