Taiwan FDA registration 5438369a3ae2fc061f2e727975b3506c
"BoschMān" Coronary Artery Dilatation Catheter
TW: "博思邁"偉鐫冠狀動脈擴張導管
Taiwan·Risk Class 3·BrosMed Medical Co., Ltd.;; BrosMed Medical B.V.·Registered Jul 22, 2022 – Jul 22, 2027ActiveRegistration details
- Analysis ID
- 5438369a3ae2fc061f2e727975b3506c
- Customs Code
- DHA09200134700
Company information
- Manufacturer
- BrosMed Medical Co., Ltd.;; BrosMed Medical B.V.
- Manufacturer Country
- Netherlands;;China
- Authorized Representative
- HAO YO ENTERPRISE CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.0005.
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Jul 22, 2022
- Expiry Date
- Jul 22, 2027
About this record
Access comprehensive regulatory information for "BoschMān" Coronary Artery Dilatation Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5438369a3ae2fc061f2e727975b3506c and manufactured by BrosMed Medical Co., Ltd.;; BrosMed Medical B.V.. The authorized representative in Taiwan is HAO YO ENTERPRISE CO., LTD..
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