Taiwan FDA registration 1f295967bb406b6f0a82cd52489d67f8
"Red" endotracheal probe (unsterilized)
TW: "雷德" 氣管內管探針 (未滅菌)
Taiwan·Risk Class 1·LAERDAL MEDICAL AS·Registered Mar 29, 2006 – Mar 29, 2011CancelledRegistration details
- Analysis ID
- 1f295967bb406b6f0a82cd52489d67f8
- Customs Code
- DHA04400324400
Company information
- Manufacturer
- LAERDAL MEDICAL AS
- Manufacturer Country
- Norway
- Authorized Representative
- Xin Yi Limited
Product details
- Intended Use
- It is limited to the first level of identification scope of the Administrative Measures for Medical Devices (endotracheal tube probe [D.5790]).
- Product Type (Level 1)
- D Anesthesiology
- Import Information
- import
Dates and status
- Registration Date
- Mar 29, 2006
- Expiry Date
- Mar 29, 2011
- Cancellation Date
- Nov 23, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Red" endotracheal probe (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1f295967bb406b6f0a82cd52489d67f8 and manufactured by LAERDAL MEDICAL AS. The authorized representative in Taiwan is Xin Yi Limited.
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