Taiwan FDA registration dadfeb81773ea96dd92282ca2e028d1f
"Katiou" Cardiovascular Surgical Instrument (Incisive)
TW: "卡蒂歐" 心臟血管外科器械 (未滅菌)
Taiwan·Risk Class 1·Cardio Surgical Ltd.;; Made (部分製程) in GERMANY·Registered Mar 21, 2024 – Mar 21, 2029ActiveRegistration details
- Analysis ID
- dadfeb81773ea96dd92282ca2e028d1f
- Customs Code
- DHA09402343002
Company information
- Manufacturer
- Cardio Surgical Ltd.;; Made (部分製程) in GERMANY
- Manufacturer Country
- Ireland;;Germany
- Authorized Representative
- INTERLINK MEDICAL ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, the first level identification range of cardiovascular surgical instruments (E.4500).
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.4500 心臟血管外科器械
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Mar 21, 2024
- Expiry Date
- Mar 21, 2029
About this record
Access comprehensive regulatory information for "Katiou" Cardiovascular Surgical Instrument (Incisive) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dadfeb81773ea96dd92282ca2e028d1f and manufactured by Cardio Surgical Ltd.;; Made (部分製程) in GERMANY. The authorized representative in Taiwan is INTERLINK MEDICAL ENTERPRISE CO., LTD..
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