Taiwan FDA registration 098c18b3a7bda96f1d31d4aa158c9e03
"Haidi Liana" hollow fibrous hemodialyzer
TW: "海帝連納"中空纖維血液透析器
Taiwan·Risk Class 2·HAIDYLENA FOR ADVANCED MEDICAL INDUSTRIES·Registered Dec 29, 2006 – Dec 29, 2016CancelledRegistration details
- Analysis ID
- 098c18b3a7bda96f1d31d4aa158c9e03
- Customs Code
- DHA00601764600
Company information
- Manufacturer
- HAIDYLENA FOR ADVANCED MEDICAL INDUSTRIES
- Manufacturer Country
- Egypt
- Authorized Representative
- PUREBLOOD-TECH INTERNATIONAL CORP.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5860 高滲透性之血液透析系統
- Import Information
- import
Dates and status
- Registration Date
- Dec 29, 2006
- Expiry Date
- Dec 29, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Haidi Liana" hollow fibrous hemodialyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 098c18b3a7bda96f1d31d4aa158c9e03 and manufactured by HAIDYLENA FOR ADVANCED MEDICAL INDUSTRIES. The authorized representative in Taiwan is PUREBLOOD-TECH INTERNATIONAL CORP..
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