Taiwan FDA registration 93ac06349f911ded8857515eed9360c9
"Ichikyoki" blood collection needle (unsterilized)
TW: “一協紀”採血針 (未滅菌)
Taiwan·Risk Class 1·HTL-STREFA S.A.·Registered Sep 20, 2019 – Sep 20, 2029ActiveRegistration details
- Analysis ID
- 93ac06349f911ded8857515eed9360c9
- Customs Code
- DHA09402088002
Company information
- Manufacturer
- HTL-STREFA S.A.
- Manufacturer Country
- Poland
- Authorized Representative
- SCHIFF INTERNATIONAL CO.
Product details
- Intended Use
- Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Sep 20, 2019
- Expiry Date
- Sep 20, 2029
About this record
Access comprehensive regulatory information for "Ichikyoki" blood collection needle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 93ac06349f911ded8857515eed9360c9 and manufactured by HTL-STREFA S.A.. The authorized representative in Taiwan is SCHIFF INTERNATIONAL CO..
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