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"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.

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810978092e2ee03e3962b7123b1c8e54
Registration Details
Taiwan FDA Registration: 810978092e2ee03e3962b7123b1c8e54
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Device Details

"Ecleris" Flexible laryngoscope (Non-Sterile)
TW: "่‰พๅ…‹่Š็†ๆ–ฏ"ๅฏๅฝŽๅผๅ–‰้ ญ้ก(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

810978092e2ee03e3962b7123b1c8e54

Ministry of Health Medical Device Import No. 019006

DHA09401900600

Company Information

United States

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

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