Taiwan FDA registration e63720afcf569570f5debc9542bdd40c
"Fujifilm" silicone self-catheter
TW: "富士"矽膠自行導尿管
Taiwan·Risk Class 2·Fuji Systems Corporation, Shirakawa Plant·Registered Jul 10, 2006 – Jul 10, 2026ExpiredRegistration details
- Analysis ID
- e63720afcf569570f5debc9542bdd40c
- Customs Code
- DHA00601685501
Company information
- Manufacturer
- Fuji Systems Corporation, Shirakawa Plant
- Manufacturer Country
- Japan
- Authorized Representative
- MING HWAY TRADING 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.5250 Urine Collector and Accessories Thereof
- Import Information
- import
Dates and status
- Registration Date
- Jul 10, 2006
- Expiry Date
- Jul 10, 2026
About this record
Access comprehensive regulatory information for "Fujifilm" silicone self-catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e63720afcf569570f5debc9542bdd40c and manufactured by Fuji Systems Corporation, Shirakawa Plant. The authorized representative in Taiwan is MING HWAY TRADING CO., LTD..
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