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"Rultract" Cardiovascular surgical instruments (Non-Sterile) - Taiwan Registration d46d1d684d11cb514364814776e9c818

Access comprehensive regulatory information for "Rultract" Cardiovascular surgical instruments (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d46d1d684d11cb514364814776e9c818 and manufactured by RULTRACT INC.. The authorized representative in Taiwan is YOO-HOO 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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d46d1d684d11cb514364814776e9c818
Registration Details
Taiwan FDA Registration: d46d1d684d11cb514364814776e9c818
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Device Details

"Rultract" Cardiovascular surgical instruments (Non-Sterile)
TW: "้ญฏๅˆ‡็‰น"ๅฟƒ่‡Ÿ่ก€็ฎกๅค–็ง‘ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d46d1d684d11cb514364814776e9c818

Ministry of Health Medical Device Import No. 015340

DHA09401534002

Company Information

United States

Product Details

Limited to the first level identification range of medical equipment management measures for cardiovascular surgical instruments (E.4500).

E Cardiovascular devices

E4500 Cardiovascular Surgical Instrument

Imported from abroad

Dates and Status

Jun 15, 2015

Jun 15, 2025