Taiwan FDA registration 95b8ead09d24913aeec0896c1035bbcc

"Ecleris" Flexible laryngoscope (Non-Sterile)

TW: "艾克萊理斯"可彎式喉頭鏡(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·ECLERIS S.R.L·Registered Aug 06, 2014 – Aug 06, 2024Expired
Registration details
Analysis ID
95b8ead09d24913aeec0896c1035bbcc
License Form
Ministry of Health Medical Device Import No. 014415
Customs Code
DHA09401441502
Company information
Manufacturer
ECLERIS S.R.L
Manufacturer Country
Argentina
Authorized Representative
BOYANG MEDICAL TECHNOLOGY CO., LTD
Product details
Intended Use
Limited to the first level of identification range of "Flexible Laryngoscope (D.5530)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1)
D Devices for anesthesiology
Product Type (Level 2)
D5530 Flexible laryngoscope
Import Information
Imported from abroad
Dates and status
Registration Date
Aug 06, 2014
Expiry Date
Aug 06, 2024
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About this record

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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