Taiwan FDA registration 08054058dfef6074fa6f1906bc73696d
“STORZ MEDICAL” Modulith SLK Lithotripter
TW: “斯拓茲”體外震波碎石機
Taiwan·Risk Class 2·MD·Storz Medical AG·Registered Jun 22, 2019 – Jun 22, 2024ExpiredRegistration details
- Analysis ID
- 08054058dfef6074fa6f1906bc73696d
- License Form
- Ministry of Health Medical Device Import No. 032694
- Customs Code
- DHA05603269401
Company information
- Manufacturer
- Storz Medical AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- KINDMED CORPORATION
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)
- H5990 Extracorporeal shock wave lithotripsy
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 22, 2019
- Expiry Date
- Jun 22, 2024
About this record
Access comprehensive regulatory information for “STORZ MEDICAL” Modulith SLK Lithotripter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 08054058dfef6074fa6f1906bc73696d and manufactured by Storz Medical AG. The authorized representative in Taiwan is KINDMED CORPORATION.
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