Taiwan FDA registration 232120c762a550f0f00a2a6adfd12c03
"Psuche" Multipurpose culture medium (Non-sterile)
TW: "安榮" 多功能培養基 (未滅菌)
Taiwan·Risk Class 1·MD·LIFEGLOBAL GROUP, LLC.·Registered Jul 08, 2015 – Jul 08, 2020CancelledRegistration details
- Analysis ID
- 232120c762a550f0f00a2a6adfd12c03
- License Form
- Ministry of Health Medical Device Import No. 015432
- Customs Code
- DHA09401543207
Company information
- Manufacturer
- LIFEGLOBAL GROUP, LLC.
- Manufacturer Country
- United States
- Authorized Representative
- PSUCHE TECHNOLOGY CO., LTD.
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C2300 Multifunctional Medium
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 08, 2015
- Expiry Date
- Jul 08, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Psuche" Multipurpose culture medium (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 232120c762a550f0f00a2a6adfd12c03 and manufactured by LIFEGLOBAL GROUP, LLC.. The authorized representative in Taiwan is PSUCHE TECHNOLOGY CO., LTD..
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