Taiwan FDA registration 74ce3e80f9e62ecbbf1f379e496692c1
"Luci" oropharyngeal airway tube (sterilized)
TW: “路希”口咽氣道管 (滅菌)
Taiwan·Risk Class 1·WILLY RUSCH GMBH·Registered Jun 24, 2013 – Jun 24, 2018CancelledRegistration details
- Analysis ID
- 74ce3e80f9e62ecbbf1f379e496692c1
- Customs Code
- DHA04401313501
Company information
- Manufacturer
- WILLY RUSCH GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN 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 Anesthesiology
- Product Type (Level 2)
- D.5110 Oropharyngeal airway tubes
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jun 24, 2013
- Expiry Date
- Jun 24, 2018
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Luci" oropharyngeal airway tube (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 74ce3e80f9e62ecbbf1f379e496692c1 and manufactured by WILLY RUSCH GMBH. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
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