Taiwan FDA registration b30f9f1b52f348bd9590b79b34213d90

Adaptive Drainage Catheter (Sterilization)

TW: 安適康導入/引流導管(滅菌)

Taiwan·Risk Class 1·Changhong Medical Materials Technology Co., Ltd.;; BenQ Materials Co., Ltd·Registered Jul 04, 2023 – Jul 04, 2028Active

Registration details

Analysis ID: b30f9f1b52f348bd9590b79b34213d90

Company information

Manufacturer: Changhong Medical Materials Technology Co., Ltd.;; BenQ Materials Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: BENQ MATERIALS CORP.

Product details

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

Dates and status

Registration Date: Jul 04, 2023
Expiry Date: Jul 04, 2028

About this record

Access comprehensive regulatory information for Adaptive 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 b30f9f1b52f348bd9590b79b34213d90 and manufactured by Changhong Medical Materials Technology Co., Ltd.;; BenQ Materials Co., Ltd. The authorized representative in Taiwan is BENQ MATERIALS CORP..

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.