Taiwan FDA registration 138c245f09b204ab18cccd57734d7417

"Meidiken sodium" suction regulator (unsterilized)

TW: “梅廸肯鈉”吸引調節器 (未滅菌)

Taiwan·Risk Class 1·TUNGSHI MEDICAL EQUIPMENT CO., LTD.·Registered Aug 05, 2013 – Aug 05, 2018Cancelled

Registration details

Analysis ID: 138c245f09b204ab18cccd57734d7417

Company information

Manufacturer: TUNGSHI MEDICAL EQUIPMENT CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: YI LIN ENTERPRISE CO., LTD.

Product details

Intended Use: Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Vacuum-powered Body Fluid Absorption Devices (J.6740)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6740 Vacuum-powered fluid absorption apparatus
Import Information: 委託製造;; 國產;; QMS/QSD

Dates and status

Registration Date: Aug 05, 2013
Expiry Date: Aug 05, 2018
Cancellation Date: Jun 16, 2022

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Meidiken sodium" suction regulator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 138c245f09b204ab18cccd57734d7417 and manufactured by TUNGSHI MEDICAL EQUIPMENT CO., LTD.. The authorized representative in Taiwan is YI LIN ENTERPRISE CO., LTD..

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