Taiwan FDA registration e70bddb5dda76e5b4093ba77cd94a540
"Weilun" rigid laryngoscope (unsterilized)
TW: "偉倫" 硬式喉頭鏡 (未滅菌)
Taiwan·Risk Class 1·WELCH ALLYN INC.·Registered Apr 08, 2020 – Apr 08, 2030ActiveRegistration details
- Analysis ID
- e70bddb5dda76e5b4093ba77cd94a540
- Customs Code
- DHA09402143104
Company information
- Manufacturer
- WELCH ALLYN INC.
- Manufacturer Country
- United States
- Authorized Representative
- Hill-Rom Taiwan Ltd.
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
- import
Dates and status
- Registration Date
- Apr 08, 2020
- Expiry Date
- Apr 08, 2030
About this record
Access comprehensive regulatory information for "Weilun" rigid laryngoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e70bddb5dda76e5b4093ba77cd94a540 and manufactured by WELCH ALLYN INC.. The authorized representative in Taiwan is Hill-Rom Taiwan Ltd..
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