Taiwan FDA registration ac6c980f84716c5d7be589e59f0ebfa4
"UE" Rigid Laryngoscope (Non-Sterile)
TW: "優異" 硬式喉頭鏡 (未滅菌)
Taiwan·Risk Class 1·MD·UE MEDICAL DEVICES, INC·Registered Jun 17, 2019 – Jun 17, 2024ExpiredRegistration details
- Analysis ID
- ac6c980f84716c5d7be589e59f0ebfa4
- License Form
- Ministry of Health Medical Device Import No. 020559
- Customs Code
- DHA09402055902
Company information
- Manufacturer
- UE MEDICAL DEVICES, INC
- Manufacturer Country
- United States
- Authorized Representative
- FRIENDS SCIENTIFIC CO., LTD.
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Rigid Laryngoscopy (D.5540)".
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5540 Rigid laryngoscope
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 17, 2019
- Expiry Date
- Jun 17, 2024
About this record
Access comprehensive regulatory information for "UE" Rigid Laryngoscope (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ac6c980f84716c5d7be589e59f0ebfa4 and manufactured by UE MEDICAL DEVICES, INC. The authorized representative in Taiwan is FRIENDS SCIENTIFIC CO., LTD..
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