Taiwan FDA registration 110e4101ba77216ebee5a5993903812c
“Plasmapp” STERLINK plasma sterilization
TW: “普拉瑪”速特力電漿滅菌機
Taiwan·Risk Class 2·MD·PLASMAPP Co., Ltd.·Registered Dec 16, 2019 – Dec 16, 2024ExpiredRegistration details
- Analysis ID
- 110e4101ba77216ebee5a5993903812c
- License Form
- Ministry of Health Medical Device Import No. 033024
- Customs Code
- DHA05603302400
Company information
- Manufacturer
- PLASMAPP Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- BIOTECH MEDICAL SCIENCE 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)
- J6860 Ethylene oxide gas sterilizer
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 16, 2019
- Expiry Date
- Dec 16, 2024
About this record
Access comprehensive regulatory information for “Plasmapp” STERLINK plasma sterilization in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 110e4101ba77216ebee5a5993903812c and manufactured by PLASMAPP Co., Ltd.. The authorized representative in Taiwan is BIOTECH MEDICAL SCIENCE CO., LTD..
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