Taiwan FDA registration d196e4b71dbf1aafd81c2f433a3acf6b
"Braun" phenanthrene intravenous indwelling needle
TW: “柏朗”菲適靜脈留置針
Taiwan·Risk Class 2·B. BRAUN MEDICAL INDUSTRIES SDN. BHD.·Registered Nov 27, 2008 – Nov 27, 2018CancelledRegistration details
- Analysis ID
- d196e4b71dbf1aafd81c2f433a3acf6b
- Customs Code
- DHA00601937604
Company information
- Manufacturer
- B. BRAUN MEDICAL INDUSTRIES SDN. BHD.
- Manufacturer Country
- Malaysia
- Authorized Representative
- B. BRAUN TAIWAN 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
- import
Dates and status
- Registration Date
- Nov 27, 2008
- Expiry Date
- Nov 27, 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 "Braun" phenanthrene 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 d196e4b71dbf1aafd81c2f433a3acf6b and manufactured by B. BRAUN MEDICAL INDUSTRIES SDN. BHD.. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..
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