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"Yoshisen" aorta punch (sterilized) - Taiwan Registration 3eae1cdf98c1948ca2a590a7eed203d5

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.

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.

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3eae1cdf98c1948ca2a590a7eed203d5
Registration Details
Taiwan FDA Registration: 3eae1cdf98c1948ca2a590a7eed203d5
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Device Details

"Yoshisen" aorta punch (sterilized)
TW: โ€œๅ‰็”Ÿโ€ไธปๅ‹•่„ˆๆ‰“ๅญ”ๅ™จ(ๆป…่Œ)
Risk Class 1

Registration Details

3eae1cdf98c1948ca2a590a7eed203d5

Company Information

Taiwan, Province of China

Product Details

Limited to the classification and grading management of medical equipment, the first level identification range of cardiovascular surgical instruments (E.4500).

E Cardiovascular Medicine Science

E.4500 ๅฟƒ่‡Ÿ่ก€็ฎกๅค–็ง‘ๅ™จๆขฐ

QMS/QSD;; ๅœ‹็”ข

Dates and Status

May 30, 2013

May 30, 2028