Taiwan FDA registration a66cee64921490d237c0941de7498de4

"Prowei" catheter needle series (sterilization)

TW: "普威"導管針系列 (滅菌)

Taiwan·Risk Class 1·Proway International Limited·Registered Apr 17, 2006 – Apr 17, 2016Cancelled

Registration details

Analysis ID: a66cee64921490d237c0941de7498de4

Company information

Manufacturer: Proway International Limited
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Proway International Limited

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: Apr 17, 2006
Expiry Date: Apr 17, 2016
Cancellation Date: Jun 28, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Prowei" catheter needle series (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a66cee64921490d237c0941de7498de4 and manufactured by Proway International Limited. The authorized representative in Taiwan is Proway International Limited.

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