Taiwan FDA registration 13f4551c43b9834b9dc7f3489a1194c3
"Optimal" non-powered, single patient use, portable suction device (sterilization)
TW: “優式”非動力式，單一病人使用，可攜帶式之抽吸器具(滅菌)
Taiwan·Risk Class 1·URESIL, LLC·Registered Aug 14, 2012 – Aug 14, 2027ActiveRegistration details
- Analysis ID
- 13f4551c43b9834b9dc7f3489a1194c3
- Customs Code
- DHA04401206205
Company information
- Manufacturer
- URESIL, LLC
- Manufacturer Country
- United States
- Authorized Representative
- MEDLIANCE LTD.
Product details
- Intended Use
- Limited to the first level of classification and grading management of medical equipment, "Non-powered, single-patient, portable suction equipment (I.4680)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4680 Non-motive, single patient-use, carry-on suctioning device
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Aug 14, 2012
- Expiry Date
- Aug 14, 2027
About this record
Access comprehensive regulatory information for "Optimal" non-powered, single patient use, portable suction device (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 13f4551c43b9834b9dc7f3489a1194c3 and manufactured by URESIL, LLC. The authorized representative in Taiwan is MEDLIANCE LTD..
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