Taiwan FDA registration 7e1eb908f52fdcef53bb2a75aa0f1278
"Mesi-drymother" platelet storage system
TW: “美斯幹母”血小板貯存系統
Taiwan·Risk Class 1·MEDIKAN CO. LTD.·Registered Jan 28, 2010 – Jan 28, 2015CancelledRegistration details
- Analysis ID
- 7e1eb908f52fdcef53bb2a75aa0f1278
- Customs Code
- DHA04400849508
Company information
- Manufacturer
- MEDIKAN CO. LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Robbie Jenny International Inc
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Containers for Preserving Platelet Concentrate (B.9575)".
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9575 Environmental control chamber for storing platelet concentrate
- Import Information
- import
Dates and status
- Registration Date
- Jan 28, 2010
- Expiry Date
- Jan 28, 2015
- Cancellation Date
- Jul 09, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Mesi-drymother" platelet storage system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7e1eb908f52fdcef53bb2a75aa0f1278 and manufactured by MEDIKAN CO. LTD.. The authorized representative in Taiwan is Robbie Jenny International Inc.
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