"Bidi" active blood collection needle - Taiwan Registration 90c6309cf010e0f4f1b02475cedcd407
Access comprehensive regulatory information for "Bidi" active blood collection needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 90c6309cf010e0f4f1b02475cedcd407 and manufactured by HTL - STREFA SP. Z.O.O.. The authorized representative in Taiwan is Taiwan Branch of American Business Bidi 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.
Device Details
Product Details
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
I General, Plastic Surgery and Dermatology
I.4800 Hand Instruments for General Surgery
import
Dates and Status
Mar 29, 2007
Mar 29, 2012
Apr 14, 2014
Cancellation Information
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