Taiwan FDA registration a9fa9b8725fa9e1b9a1b88eb4c8f1479
"Flexicare" Nasal cannula (Non-Sterile)
TW: "菲力斯可" 鼻氧管(未滅菌)
Taiwan·Risk Class 1·MD·FLEXICARE MEDICAL LIMITED.·Registered Jan 12, 2017 – Jan 12, 2027ActiveRegistration details
- Analysis ID
- a9fa9b8725fa9e1b9a1b88eb4c8f1479
- License Form
- Ministry of Health Medical Device Import No. 017408
- Customs Code
- DHA09401740807
Company information
- Manufacturer
- FLEXICARE MEDICAL LIMITED.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- HUILI MEDICAL EQUIPMENT LIMITED
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Nasal Oxygen Cannula (D.5340)".
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5340 Transnasal oxygen cannula
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 12, 2017
- Expiry Date
- Jan 12, 2027
About this record
Access comprehensive regulatory information for "Flexicare" Nasal cannula (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 a9fa9b8725fa9e1b9a1b88eb4c8f1479 and manufactured by FLEXICARE MEDICAL LIMITED.. The authorized representative in Taiwan is HUILI MEDICAL EQUIPMENT LIMITED.
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