Taiwan FDA registration fd36d62d8719089c69893eb3b68f48f2
“ENDO-FLEX” PTFE Biliary Stent
TW: “福萊克斯”膽道引流管
Taiwan·Risk Class 2·MD·ENDO-FLEX GmbH·Registered Feb 16, 2015 – Feb 16, 2025ExpiredRegistration details
- Analysis ID
- fd36d62d8719089c69893eb3b68f48f2
- License Form
- Ministry of Health Medical Device Import No. 026996
- Customs Code
- DHA05602699605
Company information
- Manufacturer
- ENDO-FLEX GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG)
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)
- H5010 Bile ductal catheters and their accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 16, 2015
- Expiry Date
- Feb 16, 2025
About this record
Access comprehensive regulatory information for “ENDO-FLEX” PTFE Biliary Stent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fd36d62d8719089c69893eb3b68f48f2 and manufactured by ENDO-FLEX GmbH. The authorized representative in Taiwan is IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG).
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