Taiwan FDA registration 6e8326598defbfcc1b301f4eb7d0dc08
Xinyi safe intravenous indwelling needle
TW: 欣意安全靜脈留置針
Taiwan·Risk Class 2·GREAT MINDS CORP.·Registered Oct 18, 2013 – Oct 18, 2018CancelledRegistration details
- Analysis ID
- 6e8326598defbfcc1b301f4eb7d0dc08
Company information
- Manufacturer
- GREAT MINDS CORP.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- MASTER & FRANK ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5200 Endovascular catheters
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Oct 18, 2013
- Expiry Date
- Oct 18, 2018
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Xinyi safe intravenous indwelling needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6e8326598defbfcc1b301f4eb7d0dc08 and manufactured by GREAT MINDS CORP.. The authorized representative in Taiwan is MASTER & FRANK ENTERPRISE CO., LTD..
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