Taiwan FDA registration 9b3d377aa5c236fe177486157770173d
“ENDO-FLEX” Guide Wires
TW: “福萊克斯”導引線
Taiwan·Risk Class 2·MD·ENDO-FLEX GmbH·Registered May 10, 2016 – May 10, 2026ExpiredRegistration details
- Analysis ID
- 9b3d377aa5c236fe177486157770173d
- License Form
- Ministry of Health Medical Device Import No. 028570
- Customs Code
- DHA05602857007
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)
- H1500 endoscope and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 10, 2016
- Expiry Date
- May 10, 2026
About this record
Access comprehensive regulatory information for “ENDO-FLEX” Guide Wires in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9b3d377aa5c236fe177486157770173d 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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