Taiwan FDA registration 75f1e3b7a01ab64d5a37a31048ec891e
"Dimak" Y-connector
TW: “迪瑪克” Y型連接器
Taiwan·Risk Class 2·Beijing Demax Medical Technology Co., Ltd.·Registered Dec 24, 2021 – Dec 24, 2026ActiveRegistration details
- Analysis ID
- 75f1e3b7a01ab64d5a37a31048ec891e
- Customs Code
- DHA09200127603
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.4290 Arterial vascular bypass surgery with contact pistons, multi-pipe connections or attachments
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Dec 24, 2021
- Expiry Date
- Dec 24, 2026
About this record
Access comprehensive regulatory information for "Dimak" Y-connector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 75f1e3b7a01ab64d5a37a31048ec891e and manufactured by Beijing Demax Medical Technology Co., Ltd.. The authorized representative in Taiwan is NO.1 BIOTECHNOLOGY CO., LTD..
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