Taiwan FDA registration 8e2c0b2a7f3559e11a66220d297b3e5e

"E-Kai" suction regulator (unsterilized)

TW: "依愷"吸引調節器(未滅菌)

Taiwan·Risk Class 1·TUNGSHI MEDICAL EQUIPMENT CO., LTD.·Registered Jul 05, 2012 – Jul 05, 2017Cancelled

Registration details

Analysis ID: 8e2c0b2a7f3559e11a66220d297b3e5e

Company information

Manufacturer: TUNGSHI MEDICAL EQUIPMENT CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: EZ-CARE INSTRUMENTS. 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: QMS/QSD;; 國產;; 委託製造

Dates and status

Registration Date: Jul 05, 2012
Expiry Date: Jul 05, 2017
Cancellation Date: Sep 19, 2016

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

Access comprehensive regulatory information for "E-Kai" 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 8e2c0b2a7f3559e11a66220d297b3e5e and manufactured by TUNGSHI MEDICAL EQUIPMENT CO., LTD.. The authorized representative in Taiwan is EZ-CARE INSTRUMENTS. CO., LTD..

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