Taiwan FDA registration 4284ff983c0812e38a2af673397fe139
"Flex" balloon expansion catheter
TW: “福萊克斯”氣球擴張導管
Taiwan·Risk Class 2·ENDO-FLEX GMBH·Registered Jul 18, 2012 – Jul 18, 2022ExpiredRegistration details
- Analysis ID
- 4284ff983c0812e38a2af673397fe139
- Customs Code
- DHA00602371400
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 and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Jul 18, 2012
- Expiry Date
- Jul 18, 2022
About this record
Access comprehensive regulatory information for "Flex" balloon expansion catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4284ff983c0812e38a2af673397fe139 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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