Taiwan FDA registration f3752044e9eec2b71ebc731f53d4f45b

Nipro Tripartite Live Plug

TW: 尼普洛三方活栓

Taiwan·Risk Class 2·Nipro Corporation Odate Factory·Registered Sep 14, 2024 – Sep 14, 2029Active

Registration details

Analysis ID: f3752044e9eec2b71ebc731f53d4f45b
Customs Code: DHA05603741305

Company information

Manufacturer: Nipro Corporation Odate Factory
Manufacturer Country: Japan
Authorized Representative: HUA CHIANG MEDICAL 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: import

Dates and status

Registration Date: Sep 14, 2024
Expiry Date: Sep 14, 2029

About this record

Access comprehensive regulatory information for Nipro Tripartite Live Plug in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f3752044e9eec2b71ebc731f53d4f45b and manufactured by Nipro Corporation Odate Factory. The authorized representative in Taiwan is HUA CHIANG MEDICAL CO., LTD..

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