Taiwan FDA registration 9de9c5fb3bc4e50c023e9fcd90df0988
"Picatech" Herpes Patch (Non-Sterile)
TW: "屏翔" 皰疹傷口保護貼(未滅菌)
Taiwan·Risk Class 1·MD·PIETRASANTA PHARMA S. P. A.·Registered Feb 12, 2020 – Feb 12, 2025ExpiredRegistration details
- Analysis ID
- 9de9c5fb3bc4e50c023e9fcd90df0988
- License Form
- Ministry of Health Medical Device Import No. 021259
- Customs Code
- DHA09402125905
Company information
- Manufacturer
- PIETRASANTA PHARMA S. P. A.
- Manufacturer Country
- Italy
- Authorized Representative
- PICATECH CO., LTD.
Product details
- Intended Use
- Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Hydrophilic Wound Covering Materials (I.4018)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4018 Hydrophilic trauma coverings
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 12, 2020
- Expiry Date
- Feb 12, 2025
About this record
Access comprehensive regulatory information for "Picatech" Herpes Patch (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 9de9c5fb3bc4e50c023e9fcd90df0988 and manufactured by PIETRASANTA PHARMA S. P. A.. The authorized representative in Taiwan is PICATECH CO., LTD..
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