"Ecleris" Flexible laryngoscope (Non-Sterile)
Taiwan·Risk Class 1·MD·ECLERIS S.R.L·Registered Apr 24, 2018 – Apr 24, 2023Expired- Analysis ID
- 810978092e2ee03e3962b7123b1c8e54
- License Form
- Ministry of Health Medical Device Import No. 019006
- Customs Code
- DHA09401900600
- Manufacturer
- ECLERIS S.R.L
- Manufacturer Country
- United States
- Authorized Representative
- BOYANG MEDICAL TECHNOLOGY CO., LTD
- 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
- Registration Date
- Apr 24, 2018
- Expiry Date
- Apr 24, 2023
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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.