Taiwan FDA registration 138a0fc3af159f82920d0f7b0e894ae4
"Sensomidi" Leila nasal cannula
TW: "仙梭美地" 萊拉鼻套管
Taiwan·Risk Class 1·SENSOR MEDICS CORPORATION·Registered Jun 22, 2005 – Jun 22, 2010CancelledRegistration details
- Analysis ID
- 138a0fc3af159f82920d0f7b0e894ae4
- Customs Code
- DHA04400018801
Company information
- Manufacturer
- SENSOR MEDICS CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- TRANSCORE TAIWAN CO., LTD.
Product details
- Intended Use
- A device that conducts gas between the ventilation tube and the patient during the patient's ventilation.
- Product Type (Level 1)
- D Anesthesiology
- Import Information
- import
Dates and status
- Registration Date
- Jun 22, 2005
- Expiry Date
- Jun 22, 2010
- Cancellation Date
- Nov 15, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Sensomidi" Leila nasal cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 138a0fc3af159f82920d0f7b0e894ae4 and manufactured by SENSOR MEDICS CORPORATION. The authorized representative in Taiwan is TRANSCORE TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices