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"Ecleris" Flexible laryngoscope (Non-Sterile) - Taiwan Registration 95b8ead09d24913aeec0896c1035bbcc

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 95b8ead09d24913aeec0896c1035bbcc 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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95b8ead09d24913aeec0896c1035bbcc
Registration Details
Taiwan FDA Registration: 95b8ead09d24913aeec0896c1035bbcc
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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

95b8ead09d24913aeec0896c1035bbcc

Ministry of Health Medical Device Import No. 014415

DHA09401441502

Company Information

Argentina

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

Aug 06, 2014

Aug 06, 2024

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