Taiwan FDA registration bd5eeed632ad55a4c4a7f4c298bbd7f8
Tripping film type liquid tripping paste (unsterilized)
TW: 流絆薄膜型液體絆創膏(未滅菌)
Taiwan·Risk Class 1·OHKI PHARMACEUTICAL CO., LTD.·Registered Apr 29, 2011 – Apr 29, 2016CancelledRegistration details
- Analysis ID
- bd5eeed632ad55a4c4a7f4c298bbd7f8
- Customs Code
- DHA04401028900
Company information
- Manufacturer
- OHKI PHARMACEUTICAL CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- TEN SUN PHARMA COMPANY LIMITED
Product details
- Intended Use
- Limit the first level identification range of liquid bandages (J.5090) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5090 Liquid bandages
- Import Information
- import
Dates and status
- Registration Date
- Apr 29, 2011
- Expiry Date
- Apr 29, 2016
- Cancellation Date
- Jul 31, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Tripping film type liquid tripping paste (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bd5eeed632ad55a4c4a7f4c298bbd7f8 and manufactured by OHKI PHARMACEUTICAL CO., LTD.. The authorized representative in Taiwan is TEN SUN PHARMA COMPANY LIMITED.
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