Taiwan FDA registration b354e85e0f9f7d0c835a5d79c54a32e3
"Fresson" Grysoe Electronic Imaging Laryngoscopy System (Unsterilized)
TW: “斐瑞頌”格萊索電子影像喉頭鏡系統(未滅菌)
Taiwan·Risk Class 1·VERATHON MEDICAL (CANADA) ULC·Registered May 17, 2007 – May 17, 2012CancelledRegistration details
- Analysis ID
- b354e85e0f9f7d0c835a5d79c54a32e3
- Customs Code
- DHA04400585905
Company information
- Manufacturer
- VERATHON MEDICAL (CANADA) ULC
- Manufacturer Country
- Canada
- Authorized Representative
- CEMMA MEDICAL CO., LTD.
Product details
- Intended Use
- Vacuum.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5540 Rigid laryngoscope
- Import Information
- import
Dates and status
- Registration Date
- May 17, 2007
- Expiry Date
- May 17, 2012
- Cancellation Date
- Apr 30, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Fresson" Grysoe Electronic Imaging Laryngoscopy System (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b354e85e0f9f7d0c835a5d79c54a32e3 and manufactured by VERATHON MEDICAL (CANADA) ULC. The authorized representative in Taiwan is CEMMA MEDICAL CO., LTD..
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