Taiwan FDA registration c5de6cc6c631b6b2d55de755d6553b2f

"Jiacheng" introduction/drainage catheter and its accessories (sterilization)

TW: “佳承” 導入/引流導管及其附件 (滅菌)

Taiwan·Risk Class 1·Jiacheng Seiko Co., Ltd. second factory·Registered Nov 09, 2012 – Nov 09, 2017Cancelled

Registration details

Analysis ID: c5de6cc6c631b6b2d55de755d6553b2f

Company information

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

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;; 國產

Dates and status

Registration Date: Nov 09, 2012
Expiry Date: Nov 09, 2017
Cancellation Date: Dec 05, 2019

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Jiacheng" introduction/drainage catheter and its accessories (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c5de6cc6c631b6b2d55de755d6553b2f and manufactured by Jiacheng Seiko Co., Ltd. second factory. The authorized representative in Taiwan is Jiacheng Seiko Co., Ltd. second factory.

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.