Taiwan FDA registration 77c1feb5ceedb19778d4adc03a3efcfc
"Flex" esophageal balloon dilation catheter
TW: “福萊克斯”食道氣球擴張導管
Taiwan·Risk Class 2·ENDO-FLEX GMBH·Registered Apr 14, 2007 – Apr 14, 2012CancelledRegistration details
- Analysis ID
- 77c1feb5ceedb19778d4adc03a3efcfc
- Customs Code
- DHA00601801901
Company information
- Manufacturer
- ENDO-FLEX GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- SHIUH-CHYNG MEDICAL CO., LTD.
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.5365 Esophageal extenders
- Import Information
- import
Dates and status
- Registration Date
- Apr 14, 2007
- Expiry Date
- Apr 14, 2012
- Cancellation Date
- Jul 25, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Flex" esophageal balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 77c1feb5ceedb19778d4adc03a3efcfc and manufactured by ENDO-FLEX GMBH. The authorized representative in Taiwan is SHIUH-CHYNG MEDICAL CO., LTD..
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