Taiwan FDA registration 6df9433025ae4d46262ff7ee3f07f58e
"Fresson" Glaiser Electronic Imaging Laryngoscopy System (Sterile/Unsterile)
TW: “斐瑞頌”格萊索電子影像喉頭鏡系統 (滅菌/未滅菌)
Taiwan·Risk Class 1·VERATHON MEDICAL (CANADA) ULC·Registered Apr 30, 2012 – Apr 30, 2027ActiveRegistration details
- Analysis ID
- 6df9433025ae4d46262ff7ee3f07f58e
- Customs Code
- DHA04401164001
Company information
- Manufacturer
- VERATHON MEDICAL (CANADA) ULC
- Manufacturer Country
- Canada
- Authorized Representative
- CEMMA MEDICAL CO., 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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Apr 30, 2012
- Expiry Date
- Apr 30, 2027
About this record
Access comprehensive regulatory information for "Fresson" Glaiser Electronic Imaging Laryngoscopy System (Sterile/Unsterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6df9433025ae4d46262ff7ee3f07f58e and manufactured by VERATHON MEDICAL (CANADA) ULC. The authorized representative in Taiwan is CEMMA MEDICAL CO., LTD..
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