Taiwan FDA registration 0268dc62e9de00e666dc996d1de50f83
"BosMě" balloon dilation catheter
TW: “博思邁”球囊擴張導管
Taiwan·Risk Class 2·BrosMed Medical Co., Ltd.;; BrosMed Medical B.V.·Registered Jul 21, 2021 – Jul 21, 2026ExpiredRegistration details
- Analysis ID
- 0268dc62e9de00e666dc996d1de50f83
- Customs Code
- DHA09200124008
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.1250 Percutaneous catheters
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Jul 21, 2021
- Expiry Date
- Jul 21, 2026
About this record
Access comprehensive regulatory information for "BosMě" balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0268dc62e9de00e666dc996d1de50f83 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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