Taiwan FDA registration b103aac13a7d193db074293a52523864

"Han Doctor Technique" Introduction and drainage catheter (sterilization)

TW: “瀚醫生技” 導入及引流導管 (滅菌)

Taiwan·Risk Class 1·Jiacheng Seiko Co., Ltd. second factory·Registered Apr 15, 2016 – Apr 15, 2021Cancelled

Registration details

Analysis ID: b103aac13a7d193db074293a52523864

Company information

Manufacturer: Jiacheng Seiko Co., Ltd. second factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Han.biomedical Inc.

Product details

Intended Use: Limited to the scope of Grade 1 identification of "Introduction/Drainage Catheters and Their Accessories (I.4200)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4200 Incoming/Drainage Tubes and Accessories
Import Information: QMS/QSD;; 委託製造;; 國產

Dates and status

Registration Date: Apr 15, 2016
Expiry Date: Apr 15, 2021
Cancellation Date: Sep 19, 2023

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Han Doctor Technique" Introduction and drainage catheter (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b103aac13a7d193db074293a52523864 and manufactured by Jiacheng Seiko Co., Ltd. second factory. The authorized representative in Taiwan is Han.biomedical Inc..

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.