Taiwan FDA registration 0126724ad96312ac9fff6f3e8da596ce
"Karst" nephroscopy
TW: “卡爾斯特”腎臟鏡
Taiwan·Risk Class 2·KARL STORZ SE & Co. KG;; Karl Storz SE & Co. KG·Registered Jan 18, 2016 – Jan 18, 2026ExpiredRegistration details
- Analysis ID
- 0126724ad96312ac9fff6f3e8da596ce
- Customs Code
- DHA05602805504
Company information
- Manufacturer
- KARL STORZ SE & Co. KG;; Karl Storz SE & Co. KG
- Manufacturer Country
- Germany
- Authorized Representative
- KARL STORZ ENDOSCOPY TAIWAN LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Jan 18, 2016
- Expiry Date
- Jan 18, 2026
About this record
Access comprehensive regulatory information for "Karst" nephroscopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0126724ad96312ac9fff6f3e8da596ce and manufactured by KARL STORZ SE & Co. KG;; Karl Storz SE & Co. KG. The authorized representative in Taiwan is KARL STORZ ENDOSCOPY TAIWAN 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