Taiwan FDA registration c4cfd32dad034a28c409548122805c5f

"Yongkang" suction regulator (unsterilized)

TW: “永康” 吸引調節器 (未滅菌)

Taiwan·Risk Class 1·YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.·Registered Apr 17, 2019 – Apr 17, 2029Active

Registration details

Analysis ID: c4cfd32dad034a28c409548122805c5f

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 classification and grading management measures for medical equipment "Vacuum-powered body fluid absorption device (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: Apr 17, 2019
Expiry Date: Apr 17, 2029

About this record

Access comprehensive regulatory information for "Yongkang" 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 c4cfd32dad034a28c409548122805c5f and manufactured by YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD..

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.