Taiwan FDA registration 012ac39f6b750d85437e6cba3a9802c3
"Medtronic" rigid laryngoscope (unsterilized)
TW: “美敦力”硬式喉頭鏡（未滅菌）
Taiwan·Risk Class 1·MEDTRONIC XOMED INSTRUMENTATION SAS·Registered Mar 08, 2010 – Mar 08, 2020CancelledRegistration details
- Analysis ID
- 012ac39f6b750d85437e6cba3a9802c3
- Customs Code
- DHA04400860706
Company information
- Manufacturer
- MEDTRONIC XOMED INSTRUMENTATION SAS
- Manufacturer Country
- France
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Rigid Laryngoscopy (D.5540)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5540 Rigid laryngoscope
- Import Information
- import
Dates and status
- Registration Date
- Mar 08, 2010
- Expiry Date
- Mar 08, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Medtronic" rigid laryngoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 012ac39f6b750d85437e6cba3a9802c3 and manufactured by MEDTRONIC XOMED INSTRUMENTATION SAS. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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