Taiwan FDA registration f91567f06c1fb8223dce79bd3944aacf
"Filisco" rigid laryngoscope (sterilized)
TW: "菲力斯可" 硬式喉頭鏡 (滅菌)
Taiwan·Risk Class 1·FLEXICARE MEDICAL LIMITED.·Registered Oct 19, 2020 – Oct 19, 2025ExpiredRegistration details
- Analysis ID
- f91567f06c1fb8223dce79bd3944aacf
- Customs Code
- DHA09402204300
Company information
- Manufacturer
- FLEXICARE MEDICAL LIMITED.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- HUILI MEDICAL EQUIPMENT LIMITED
Product details
- Intended Use
- Limited to the first level identification range of the "rigid laryngoscope (D.5540)" of the Measures for the Classification and Grading Management of Medical Devices.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5540 Rigid laryngoscope
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Oct 19, 2020
- Expiry Date
- Oct 19, 2025
About this record
Access comprehensive regulatory information for "Filisco" rigid laryngoscope (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f91567f06c1fb8223dce79bd3944aacf and manufactured by FLEXICARE MEDICAL LIMITED.. The authorized representative in Taiwan is HUILI MEDICAL EQUIPMENT LIMITED.
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices