Taiwan FDA registration dda4201e01b8d06b7f04a4fa6fef8c18
“ENDO-FLEX” Self-Expanding Nitinol Stents
TW: “福萊克斯”十二指腸-結腸/直腸自擴式支架系統
Taiwan·Risk Class 2·MD·ENDO-FLEX GmbH·Registered Sep 18, 2013 – Sep 18, 2023ExpiredRegistration details
- Analysis ID
- dda4201e01b8d06b7f04a4fa6fef8c18
- License Form
- Ministry of Health Medical Device Import No. 025473
- Customs Code
- DHA05602547307
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)
- I General and plastic surgical devices
- Product Type (Level 2)
- I3610 Esophageal supplements
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 18, 2013
- Expiry Date
- Sep 18, 2023
About this record
Access comprehensive regulatory information for “ENDO-FLEX” Self-Expanding Nitinol Stents in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dda4201e01b8d06b7f04a4fa6fef8c18 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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