"Teleflex" Medicinal nonventilatorynebulizer (atomizer) (Non-Sterile)
Taiwan·Risk Class 1·MD·Hudson Respiratory Care Tecate S.de R.L.de C.V.(A Teleflex Medical Company)·Registered May 31, 2018 – May 31, 2023Expired- Analysis ID
- 578fd56dcc1f32c0cfbaa02a54dd60c2
- License Form
- Ministry of Health Medical Device Import No. 019116
- Customs Code
- DHA09401911604
- Manufacturer Country
- Mexico
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN LTD.
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-respiratory Medical Aerosol Device (D.5640)".
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5640 Non-respiratory medical nebulizer
- Import Information
- Imported from abroad
- Registration Date
- May 31, 2018
- Expiry Date
- May 31, 2023
Access comprehensive regulatory information for "Teleflex" Medicinal nonventilatorynebulizer (atomizer) (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 578fd56dcc1f32c0cfbaa02a54dd60c2 and manufactured by Hudson Respiratory Care Tecate S.de R.L.de C.V.(A Teleflex Medical Company). The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
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