Taiwan FDA registration d096d3f91de76e1adf1b8e8d6013039b
“Teleflex” Gibeck Humid-Vent HMEF
TW: “泰利福”吉倍克細菌病毒過濾潮濕球
Taiwan·Risk Class 2·MD·Teleflex Medical Sdn.Bhd.·Registered Jan 04, 2019 – Jan 04, 2024ExpiredRegistration details
- Analysis ID
- d096d3f91de76e1adf1b8e8d6013039b
- License Form
- Ministry of Health Medical Device Import No. 032060
- Customs Code
- DHA05603206002
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)
- D5260 Breathing line bacterial filter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 04, 2019
- Expiry Date
- Jan 04, 2024
About this record
Access comprehensive regulatory information for “Teleflex” Gibeck Humid-Vent HMEF in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d096d3f91de76e1adf1b8e8d6013039b and manufactured by Teleflex Medical Sdn.Bhd.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
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