Taiwan FDA registration 741d6d1f9f2e2712505415a839d85dae
"Vertical Spin" powder medium (unsterilized)
TW: 〝立飛旋〞粉末培養基 (未滅菌)
Registration details
- Analysis ID
- 741d6d1f9f2e2712505415a839d85dae
- Customs Code
- DHA04401073303
Company information
- Manufacturer
- LIOFILCHEM S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- DYBO ENTERPRISE COMPANY LIMITED
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Selective Media (C.2360)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.2360 選擇性培養基
- Import Information
- import
Dates and status
- Registration Date
- Aug 22, 2011
- Expiry Date
- Aug 22, 2016
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Vertical Spin" powder medium (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 741d6d1f9f2e2712505415a839d85dae and manufactured by LIOFILCHEM S.R.L.. The authorized representative in Taiwan is DYBO ENTERPRISE COMPANY LIMITED.
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