Taiwan FDA registration af6cfde1c9816e8d10362682dd367bf9
Prismaflo IIS Blood Warmer
TW: “普利斯馬”血液加溫器
Taiwan·Risk Class 2·MD·Stihler Electronic GmbH·Registered Jan 31, 2018 – Jan 31, 2023ExpiredRegistration details
- Analysis ID
- af6cfde1c9816e8d10362682dd367bf9
- License Form
- Ministry of Health Medical Device Import No. 030847
- Customs Code
- DHA05603084703
Company information
- Manufacturer
- Stihler Electronic GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- BAXTER HEALTHCARE LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H5820 Hemodialysis systems and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 31, 2018
- Expiry Date
- Jan 31, 2023
About this record
Access comprehensive regulatory information for Prismaflo IIS Blood Warmer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number af6cfde1c9816e8d10362682dd367bf9 and manufactured by Stihler Electronic GmbH. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..
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