Taiwan FDA registration 64ce68794ab5c32367039d79125a0153
"Mei Ariel" Substance Abuse Liquid (Unsterilized).
TW: “美艾利爾”揣耶濟 藥物濫用品管液(未滅菌) 。
Registration details
- Analysis ID
- 64ce68794ab5c32367039d79125a0153
- Customs Code
- DHA04401258600
Company information
- Manufacturer
- ALERE SAN DIEGO, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Ariel Health Inc
Product details
- Intended Use
- Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- import
Dates and status
- Registration Date
- Jan 11, 2013
- Expiry Date
- Jan 11, 2018
- Cancellation Date
- Nov 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Mei Ariel" Substance Abuse Liquid (Unsterilized). in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 64ce68794ab5c32367039d79125a0153 and manufactured by ALERE SAN DIEGO, INC.. The authorized representative in Taiwan is Ariel Health Inc.
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