Taiwan FDA registration 5491ddcfb4ab606a063f433901c8e18c
"Mercury" OROPHARYNGEAL AIRWAY (Non-Sterile)
TW: "莫可瑞" 口咽氣道管 (未滅菌)
Taiwan·Risk Class 1·MD·MERCURY MEDICAL·Registered Dec 28, 2017 – Dec 28, 2022ExpiredRegistration details
- Analysis ID
- 5491ddcfb4ab606a063f433901c8e18c
- License Form
- Ministry of Health Medical Device Import No. 018664
- Customs Code
- DHA09401866404
Company information
- Manufacturer
- MERCURY MEDICAL
- Manufacturer Country
- United States
- Authorized Representative
- FRIENDS SCIENTIFIC CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the oropharyngeal airway tube (D.5110) for the management of medical devices.
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5110 Oropharyngeal airway tube
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 28, 2017
- Expiry Date
- Dec 28, 2022
About this record
Access comprehensive regulatory information for "Mercury" OROPHARYNGEAL AIRWAY (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 5491ddcfb4ab606a063f433901c8e18c and manufactured by MERCURY MEDICAL. The authorized representative in Taiwan is FRIENDS SCIENTIFIC CO., LTD..
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