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"Maquet" Cardiovascular Surgical Instruments (Non-Sterile) - Taiwan Registration c64510d5c37bd95bf30899654d2ed3f3

Access comprehensive regulatory information for "Maquet" 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 c64510d5c37bd95bf30899654d2ed3f3 and manufactured by MAQUET CARDIOVASCULAR LLC. The authorized representative in Taiwan is PRO-READY ENTERPRISE 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.

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c64510d5c37bd95bf30899654d2ed3f3
Registration Details
Taiwan FDA Registration: c64510d5c37bd95bf30899654d2ed3f3
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Device Details

"Maquet" Cardiovascular Surgical Instruments (Non-Sterile)
TW: "้ฆฌๅ…‹"ๅฟƒ่‡Ÿ่ก€็ฎกๅค–็ง‘ๅ™จๆขฐ(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

c64510d5c37bd95bf30899654d2ed3f3

Ministry of Health Medical Device Import No. 014610

DHA09401461000

Company Information

United States

Product Details

E Cardiovascular devices

E4500 Cardiovascular Surgical Instrument

Imported from abroad

Dates and Status

Oct 27, 2014

Oct 27, 2019

Jun 16, 2022

Cancellation Information

Logged out

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