Taiwan FDA registration b4a767df37a6bf3678d1f60299ed84ae
"Hosiby" inner tube wing needle
TW: “好思比”內廔管翼狀針
Taiwan·Risk Class 2·HOSPITECH MANUFACTURING SERVICES SDN BHD·Registered Jan 30, 2008 – Jan 30, 2018CancelledRegistration details
- Analysis ID
- b4a767df37a6bf3678d1f60299ed84ae
- Customs Code
- DHA00601857202
Company information
- Manufacturer
- HOSPITECH MANUFACTURING SERVICES SDN BHD
- Manufacturer Country
- Malaysia
- Authorized Representative
- DORA MEDICAL EQUIPMENT 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.5540 Blood Access Devices and Accessories
- Import Information
- import
Dates and status
- Registration Date
- Jan 30, 2008
- Expiry Date
- Jan 30, 2018
- Cancellation Date
- Nov 28, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Hosiby" inner tube wing needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b4a767df37a6bf3678d1f60299ed84ae and manufactured by HOSPITECH MANUFACTURING SERVICES SDN BHD. The authorized representative in Taiwan is DORA MEDICAL EQUIPMENT CO., LTD..
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