Taiwan FDA registration f813310e19a4e8d99080e01ac7827415
Xinbo" Otoscope (Non-sterile)
TW: "鑫博"耳鏡(未滅菌)
Registration details
- Analysis ID
- f813310e19a4e8d99080e01ac7827415
- License Form
- Ministry of Health Medical Device Import No. 018827
- Customs Code
- DHA09401882706
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 "Otoscope (G.4770)".
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4770 Otoscope
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 22, 2018
- Expiry Date
- Feb 22, 2023
About this record
Access comprehensive regulatory information for Xinbo" Otoscope (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 f813310e19a4e8d99080e01ac7827415 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.
Free DatabasePowered by Pure Global AI89,000+ Devices