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"GOODMORNING" Capillary Blood Collection Tube (Non-Sterile) - Taiwan Registration 040afb7a8e341ef5c1234bc0db7dcd78

Access comprehensive regulatory information for "GOODMORNING" Capillary Blood Collection Tube (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 040afb7a8e341ef5c1234bc0db7dcd78 and manufactured by GOODMORNING BIO CO., LTD.. The authorized representative in Taiwan is Sung Ann Medical Equipment .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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040afb7a8e341ef5c1234bc0db7dcd78
Registration Details
Taiwan FDA Registration: 040afb7a8e341ef5c1234bc0db7dcd78
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Device Details

"GOODMORNING" Capillary Blood Collection Tube (Non-Sterile)
TW: "ๅ›บๅพ—ๆž—"ๆฏ›็ดฐ่ก€ๆถฒๆ”ถ้›†็ฎก(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

040afb7a8e341ef5c1234bc0db7dcd78

Ministry of Health Medical Device Import No. 014330

DHA09401433007

Company Information

Korea, Republic of

Product Details

B Hematology and pathology devices

B6150 Capillary blood collection tube

Imported from abroad

Dates and Status

Jul 15, 2014

Jul 15, 2019

Aug 11, 2015

Cancellation Information

Logged out

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