Taiwan FDA registration d75704df2f3dc6a158d2ff5c255dbf13
"Ji Ai" Sspotte endoscopic marking liquid
TW: "吉愛" 史斑特內視鏡記號液
Registration details
- Analysis ID
- d75704df2f3dc6a158d2ff5c255dbf13
- Customs Code
- DHA00601105802
Company information
- Manufacturer
- GI SUPPLY
- Manufacturer Country
- United States
- Authorized Representative
- Tronmed CO., 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
- Feb 22, 2005
- Expiry Date
- Feb 22, 2030
About this record
Access comprehensive regulatory information for "Ji Ai" Sspotte endoscopic marking liquid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d75704df2f3dc6a158d2ff5c255dbf13 and manufactured by GI SUPPLY. The authorized representative in Taiwan is Tronmed 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