Taiwan FDA registration b49f480aa0d0521e4d04916cebc11a60
“RAYBOW” Fiberoptic Dental Light Source (Non-Sterile)
TW: “瑞寶”光纖維牙科用光源 (未滅菌)
Taiwan·Risk Class 1·MD·RAYBOW GMBH·Registered Dec 31, 2013 – Dec 31, 2018CancelledRegistration details
- Analysis ID
- b49f480aa0d0521e4d04916cebc11a60
- License Form
- Ministry of Health Medical Device Import No. 013739
- Customs Code
- DHA09401373900
Company information
- Manufacturer
- RAYBOW GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- PULLIER CO., LTD.
Product details
- 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
- Dec 31, 2013
- Expiry Date
- Dec 31, 2018
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “RAYBOW” Fiberoptic Dental Light Source (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 b49f480aa0d0521e4d04916cebc11a60 and manufactured by RAYBOW GMBH. The authorized representative in Taiwan is PULLIER 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