Taiwan FDA registration 77a11a8c0c5b8679980495d771db6c92
"Fresson" Grysoe Electronic Imaging Laryngoscopy System (Sterilization)
TW: “斐瑞頌”格萊索電子影像喉頭鏡系統 (滅菌)
Taiwan·Risk Class 1·VERATHON MEDICAL (CANADA) ULC·Registered Oct 21, 2008 – Oct 21, 2013CancelledRegistration details
- Analysis ID
- 77a11a8c0c5b8679980495d771db6c92
- Customs Code
- DHA04400715202
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 of identification range of "rigid laryngoscopy (D.5540)" and "endotracheal probe (D.5790)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5540 硬式喉頭鏡;; D.5790 氣管內管探針
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Oct 21, 2008
- Expiry Date
- Oct 21, 2013
- Cancellation Date
- Jan 09, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Fresson" Grysoe Electronic Imaging Laryngoscopy System (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 77a11a8c0c5b8679980495d771db6c92 and manufactured by VERATHON MEDICAL (CANADA) ULC. The authorized representative in Taiwan is CEMMA MEDICAL CO., LTD..
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