Taiwan FDA registration a502741730237371d29986237cabf305
"Meibo" infusion sleeve
TW: “美博”輸液套
Taiwan·Risk Class 2·MEDPRO INTERNATIONAL (THAILAND) LTD.·Registered Jul 10, 2007 – Jul 10, 2012CancelledRegistration details
- Analysis ID
- a502741730237371d29986237cabf305
- Customs Code
- DHA00601815802
Company information
- Manufacturer
- MEDPRO INTERNATIONAL (THAILAND) LTD.
- Manufacturer Country
- Thailand
- Authorized Representative
- FISOMED TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5430 非電動式液體注射器
- Import Information
- import
Dates and status
- Registration Date
- Jul 10, 2007
- Expiry Date
- Jul 10, 2012
- Cancellation Date
- Jul 25, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Meibo" infusion sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a502741730237371d29986237cabf305 and manufactured by MEDPRO INTERNATIONAL (THAILAND) LTD.. The authorized representative in Taiwan is FISOMED TAIWAN CO., LTD..
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