"Ecleris" Flexible laryngoscope (Non-Sterile) - Taiwan Registration 810978092e2ee03e3962b7123b1c8e54
Access comprehensive regulatory information for "Ecleris" Flexible laryngoscope (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 810978092e2ee03e3962b7123b1c8e54 and manufactured by ECLERIS S.R.L. The authorized representative in Taiwan is BOYANG MEDICAL TECHNOLOGY CO., LTD.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ECLERIS S.R.L, and 1 recent registrations in the same category. 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
Registration Details
810978092e2ee03e3962b7123b1c8e54
Ministry of Health Medical Device Import No. 019006
DHA09401900600
Product Details
Limited to the first level of identification range of "Flexible Laryngoscope (D.5530)" under the Measures for the Administration of Medical Devices.
D Devices for anesthesiology
D5530 Flexible laryngoscope
Imported from abroad
Dates and Status
Apr 24, 2018
Apr 24, 2023

