Taiwan FDA registration bc07df3ea199f10afcb560f753f4a340
“Rudolf” Uretero-Renoscopy
TW: “魯道夫”輸尿管鏡
Taiwan·Risk Class 2·MD·RUDOLF MEDICAL GMBH + CO. KG·Registered Aug 07, 2015 – Aug 07, 2025ExpiredRegistration details
- Analysis ID
- bc07df3ea199f10afcb560f753f4a340
- License Form
- Ministry of Health Medical Device Import No. 027625
- Customs Code
- DHA05602762501
Company information
- Manufacturer
- RUDOLF MEDICAL GMBH + CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- EVERMED INTERNATIONAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H1500 endoscope and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 07, 2015
- Expiry Date
- Aug 07, 2025
About this record
Access comprehensive regulatory information for “Rudolf” Uretero-Renoscopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bc07df3ea199f10afcb560f753f4a340 and manufactured by RUDOLF MEDICAL GMBH + CO. KG. The authorized representative in Taiwan is EVERMED INTERNATIONAL 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