Taiwan FDA registration dec564e680214d8b3f6fc76fc0a34499
“Gambro” Revaclear
TW: “衛寶”血液透析器
Taiwan·Risk Class 2·MD·GAMBRO DIALYSATOREN GMBH·Registered Oct 09, 2013 – Oct 09, 2028ActiveRegistration details
- Analysis ID
- dec564e680214d8b3f6fc76fc0a34499
- License Form
- Ministry of Health Medical Device Import No. 025491
- Customs Code
- DHA05602549109
Company information
- Manufacturer
- GAMBRO DIALYSATOREN 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)
- H5860 Highly permeable hemodialysis system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 09, 2013
- Expiry Date
- Oct 09, 2028
About this record
Access comprehensive regulatory information for “Gambro” Revaclear in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dec564e680214d8b3f6fc76fc0a34499 and manufactured by GAMBRO DIALYSATOREN GMBH. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..
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