Taiwan FDA registration b677571b76ed7e4cb3a7289695c2f43c
Tokyo Koshisha Liquid Plaster (Non-Sterile)
TW: 東京甲子社液體OK繃(未滅菌)
Taiwan·Risk Class 1·MD·TOKYO KOSHISHA CO., LTD.·Registered Feb 19, 2021 – Feb 19, 2026ExpiredRegistration details
- Analysis ID
- b677571b76ed7e4cb3a7289695c2f43c
- License Form
- Ministry of Health Medical Device Import No. 022316
- Customs Code
- DHA09402231609
Company information
- Manufacturer
- TOKYO KOSHISHA CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- KWANG HWA DRUG FACTORY
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)
- J5090 Liquid bandages
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 19, 2021
- Expiry Date
- Feb 19, 2026
About this record
Access comprehensive regulatory information for Tokyo Koshisha Liquid Plaster (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 b677571b76ed7e4cb3a7289695c2f43c and manufactured by TOKYO KOSHISHA CO., LTD.. The authorized representative in Taiwan is KWANG HWA DRUG FACTORY.
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