Taiwan FDA registration 8f1105c1b49f9706edab2749cb5769e0
"Intesco" endotracheal probe (sterilized)
TW: “茵特斯克” 氣管內管探針(滅菌)
Taiwan·Risk Class 1·JSC Intersurgical·Registered Jun 17, 2023 – Jun 17, 2028ActiveRegistration details
- Analysis ID
- 8f1105c1b49f9706edab2749cb5769e0
- Customs Code
- DHA09402315200
Company information
- Manufacturer
- JSC Intersurgical
- Manufacturer Country
- Lithuania
- Authorized Representative
- INTERSURGICAL TAIWAN LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "endotracheal tube probe (D.5790)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5790 氣管內管探針
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jun 17, 2023
- Expiry Date
- Jun 17, 2028
About this record
Access comprehensive regulatory information for "Intesco" endotracheal probe (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8f1105c1b49f9706edab2749cb5769e0 and manufactured by JSC Intersurgical. The authorized representative in Taiwan is INTERSURGICAL TAIWAN LTD..
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