Taiwan FDA registration 3eae1cdf98c1948ca2a590a7eed203d5

"Yoshisen" aorta punch (sterilized)

TW: “吉生”主動脈打孔器(滅菌)

Taiwan·Risk Class 1·JI SHENG MEDICAL COMPANY LIMITED·Registered May 30, 2013 – May 30, 2028Active

Registration details

Analysis ID: 3eae1cdf98c1948ca2a590a7eed203d5

Company information

Manufacturer: JI SHENG MEDICAL COMPANY LIMITED
Manufacturer Country: Taiwan, Province of China
Authorized Representative: JI SHENG MEDICAL COMPANY LIMITED

Product details

Intended Use: Limited to the classification and grading management of medical equipment, the first level identification range of cardiovascular surgical instruments (E.4500).
Product Type (Level 1): E Cardiovascular Medicine Science
Product Type (Level 2): E.4500 心臟血管外科器械
Import Information: QMS/QSD;; 國產

Dates and status

Registration Date: May 30, 2013
Expiry Date: May 30, 2028

About this record

Access comprehensive regulatory information for "Yoshisen" aorta punch (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3eae1cdf98c1948ca2a590a7eed203d5 and manufactured by JI SHENG MEDICAL COMPANY LIMITED. The authorized representative in Taiwan is JI SHENG MEDICAL COMPANY LIMITED.

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