Taiwan FDA registration 7fb95faff85071ab42a0f00fa22e2e32
“Teleflex” PercuQuick Set
TW: “泰利福” 快速經皮氣切組及配件
Taiwan·Risk Class 2·MD·Teleflex Medical Sdn.Bhd.·Registered Apr 15, 2014 – Apr 15, 2024ExpiredRegistration details
- Analysis ID
- 7fb95faff85071ab42a0f00fa22e2e32
- License Form
- Ministry of Health Medical Device Import No. 026101
- Customs Code
- DHA05602610101
Company information
- Manufacturer
- Teleflex Medical Sdn.Bhd.
- Manufacturer Country
- Malaysia
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5800 Trachetomy tube and its balloon
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 15, 2014
- Expiry Date
- Apr 15, 2024
About this record
Access comprehensive regulatory information for “Teleflex” PercuQuick Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7fb95faff85071ab42a0f00fa22e2e32 and manufactured by Teleflex Medical Sdn.Bhd.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
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