Taiwan FDA registration 888d58f0bbe08b7c6c1d38f9c0775185

"Dimak" multi-way connector

TW: “迪瑪克” 多路連接器

Taiwan·Risk Class 2·Beijing Demax Medical Technology Co., Ltd.·Registered Dec 24, 2021 – Dec 24, 2026Active

Registration details

Analysis ID: 888d58f0bbe08b7c6c1d38f9c0775185
Customs Code: DHA09200127501

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: Input;; Chinese goods

Dates and status

Registration Date: Dec 24, 2021
Expiry Date: Dec 24, 2026

About this record

Access comprehensive regulatory information for "Dimak" multi-way connector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 888d58f0bbe08b7c6c1d38f9c0775185 and manufactured by Beijing Demax Medical Technology Co., Ltd.. The authorized representative in Taiwan is NO.1 BIOTECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.