Taiwan FDA registration 13ef73e0b764cd4f0102654ed20a0c34
"Dimak" balloon dilation pressostat
TW: “迪瑪克” 球囊擴張加壓器
Taiwan·Risk Class 2·Beijing Demax Medical Technology Co., Ltd.·Registered Sep 22, 2021 – Sep 22, 2026ActiveRegistration details
- Analysis ID
- 13ef73e0b764cd4f0102654ed20a0c34
- Customs Code
- DHA09200126103
Company information
- Manufacturer
- Beijing Demax Medical Technology Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- NO.1 BIOTECHNOLOGY 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.1650 血管攝影注射器和注射筒
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Sep 22, 2021
- Expiry Date
- Sep 22, 2026
About this record
Access comprehensive regulatory information for "Dimak" balloon dilation pressostat in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 13ef73e0b764cd4f0102654ed20a0c34 and manufactured by Beijing Demax Medical Technology Co., Ltd.. The authorized representative in Taiwan is NO.1 BIOTECHNOLOGY CO., LTD..
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