Taiwan FDA registration e8242c45097be9c83fefd2ecce7883ef
"Leinset" disposable electronic bile duct endoscope and its accessories
TW: “萊恩瑟特”一次性使用電子膽管內視鏡及其附件
Registration details
- Analysis ID
- e8242c45097be9c83fefd2ecce7883ef
- Customs Code
- DHA09200149400
Company information
- Manufacturer
- Hangzhou Lancetinc Medical Technology Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- CANASONIC CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Oct 11, 2023
- Expiry Date
- Oct 11, 2028
About this record
Access comprehensive regulatory information for "Leinset" disposable electronic bile duct endoscope and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e8242c45097be9c83fefd2ecce7883ef and manufactured by Hangzhou Lancetinc Medical Technology Co., Ltd.. The authorized representative in Taiwan is CANASONIC 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