Taiwan FDA registration d60b0e2a5e769b3cbe803c80b93f5dfb
“GaleMed” Oropharyngeal Airway (Non-Sterile)
TW: “崇仁” 口咽氣道管器材（未滅菌）
Taiwan·Risk Class 1·MD·GALEMED (XIAMEN) CO., LTD.·Registered Dec 27, 2019 – Dec 27, 2024ExpiredRegistration details
- Analysis ID
- d60b0e2a5e769b3cbe803c80b93f5dfb
- License Form
- Ministry of Health Medical Device Land Transport No. 004062
- Customs Code
- DHA09600406205
Company information
- Manufacturer
- GALEMED (XIAMEN) CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- GALEMED CORPORATION
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; Made in China
Dates and status
- Registration Date
- Dec 27, 2019
- Expiry Date
- Dec 27, 2024
About this record
Access comprehensive regulatory information for “GaleMed” 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 d60b0e2a5e769b3cbe803c80b93f5dfb and manufactured by GALEMED (XIAMEN) CO., LTD.. The authorized representative in Taiwan is GALEMED CORPORATION.
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