Taiwan FDA registration b76d18ab3be3d8950ea4d976ef570f21
"Flex" bracket placement kit
TW: “福萊克斯”支架放置套組
Taiwan·Risk Class 2·ENDO-FLEX GMBH·Registered May 12, 2009 – May 12, 2024ExpiredRegistration details
- Analysis ID
- b76d18ab3be3d8950ea4d976ef570f21
- Customs Code
- DHA00601984401
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.5010 膽管用導管及其附件
- Import Information
- import
Dates and status
- Registration Date
- May 12, 2009
- Expiry Date
- May 12, 2024
About this record
Access comprehensive regulatory information for "Flex" bracket placement kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b76d18ab3be3d8950ea4d976ef570f21 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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