Taiwan FDA registration 2d8a6340bdd60ec3aef75b74cea78e26
“Nipro” Disposable Arterial Venous Fistula Set (BioHole, Dull Needle)
TW: “尼普洛”內瘻管翼狀針(鈍針)
Taiwan·Risk Class 2·MD·Nipro (Thailand) Corporation Limited·Registered Sep 10, 2013 – Sep 10, 2028ActiveRegistration details
- Analysis ID
- 2d8a6340bdd60ec3aef75b74cea78e26
- License Form
- Ministry of Health Medical Device Import No. 025406
- Customs Code
- DHA05602540605
Company information
- Manufacturer
- Nipro (Thailand) Corporation Limited
- Manufacturer Country
- Thailand
- Authorized Representative
- HUA CHIANG MEDICAL CO., 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)
- H5540 Blood access devices and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 10, 2013
- Expiry Date
- Sep 10, 2028
About this record
Access comprehensive regulatory information for “Nipro” Disposable Arterial Venous Fistula Set (BioHole, Dull Needle) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2d8a6340bdd60ec3aef75b74cea78e26 and manufactured by Nipro (Thailand) Corporation Limited. The authorized representative in Taiwan is HUA CHIANG MEDICAL CO., LTD..
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