Taiwan FDA registration 596906db0294afab7fc317627fb04f2a
Percutaneous nephrostomy group "West Mexi"
TW: 經皮腎臟造廔組"西美西"
Taiwan·Risk Class 2·CREATE MEDICCO., LTD. HOKKAIDO PLANT·Registered Dec 08, 1994 – Feb 09, 2019CancelledRegistration details
- Analysis ID
- 596906db0294afab7fc317627fb04f2a
- Customs Code
- DHA00600737703
Company information
- Manufacturer
- CREATE MEDICCO., LTD. HOKKAIDO PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- CHINA HOSMED INTERNATIONAL INC.
Product details
- Product Type (Level 1)
- 0601 Intensive Care Unit and Cardiac Intensive Care Unit Equipment
- Import Information
- import
Dates and status
- Registration Date
- Dec 08, 1994
- Expiry Date
- Feb 09, 2019
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Percutaneous nephrostomy group "West Mexi" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 596906db0294afab7fc317627fb04f2a and manufactured by CREATE MEDICCO., LTD. HOKKAIDO PLANT. The authorized representative in Taiwan is CHINA HOSMED INTERNATIONAL INC..
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