"Elkafort" one-time laryngoscope blade (sterilized) - Taiwan Registration 9991a1f9e81f7171a9751848d8e9d283
Access comprehensive regulatory information for "Elkafort" one-time laryngoscope blade (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9991a1f9e81f7171a9751848d8e9d283 and manufactured by Xubang Medical Equipment Co., Ltd. The authorized representative in Taiwan is Xubang Medical Equipment 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 of identification scope of the Measures for the Administration of Medical Devices "Rigid Laryngoscopy (D.5540)".
D Anesthesiology
D.5540 Rigid laryngoscope
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Dates and Status
Jul 02, 2013
Jul 02, 2023
Apr 08, 2019
Cancellation Information
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