Taiwan FDA registration d558fae62c8a9d2f7708c4b75709f794

"Yongkang" waste liquid collection bag (unsterilized)

TW: "永康" 廢液收集袋 (未滅菌)

Taiwan·Risk Class 1·YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.·Registered Aug 03, 2017 – Aug 03, 2022Cancelled

Registration details

Analysis ID: d558fae62c8a9d2f7708c4b75709f794

Company information

Manufacturer: YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: YUNG KANG MEDICAL DEVICE TECHNOLOGY 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

Dates and status

Registration Date: Aug 03, 2017
Expiry Date: Aug 03, 2022
Cancellation Date: Apr 12, 2024

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Yongkang" waste liquid collection bag (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d558fae62c8a9d2f7708c4b75709f794 and manufactured by YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD..

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