Taiwan FDA registration a541ec2fe695cbcc459e6512dc0e191b
“Rusch” Silkoclear tracheal Tube
TW: “路希”矽膠製氣管內管
Taiwan·Risk Class 2·MD·Teleflex Medical Sdn.Bhd.·Registered Oct 24, 2014 – Oct 24, 2019CancelledRegistration details
- Analysis ID
- a541ec2fe695cbcc459e6512dc0e191b
- License Form
- Ministry of Health Medical Device Import No. 026595
- Customs Code
- DHA05602659500
Company information
- Manufacturer
- Teleflex Medical Sdn.Bhd.
- Manufacturer Country
- Malaysia
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN LTD.
Product details
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5730 Endotracheal tube
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 24, 2014
- Expiry Date
- Oct 24, 2019
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “Rusch” Silkoclear tracheal Tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a541ec2fe695cbcc459e6512dc0e191b and manufactured by Teleflex Medical Sdn.Bhd.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
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