Taiwan FDA registration b26e65263d11151ad22ad0719a62056e

“DPB” Cannula

TW: “呈汝” 鈍針

Taiwan·Risk Class 2·MD·Dashun Factory of Chengru Biotechnology Co., Ltd·Registered Aug 14, 2023 – Aug 14, 2028Active

Registration details

Analysis ID: b26e65263d11151ad22ad0719a62056e
License Form: Ministry of Health Medical Device Manufacturing No. 007961

Company information

Manufacturer: Dashun Factory of Chengru Biotechnology Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: DERMATO PLASTICA BEAUTY CO., LTD.

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J5570 Subcutaneous single-lumen needle
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Aug 14, 2023
Expiry Date: Aug 14, 2028

About this record

Access comprehensive regulatory information for “DPB” Cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b26e65263d11151ad22ad0719a62056e and manufactured by Dashun Factory of Chengru Biotechnology Co., Ltd. The authorized representative in Taiwan is DERMATO PLASTICA BEAUTY CO., LTD..

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