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“Nipro” Disposable Arterial Venous Fistula Set (BioHole, Dull Needle) - Taiwan Registration 2d8a6340bdd60ec3aef75b74cea78e26

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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2d8a6340bdd60ec3aef75b74cea78e26
Registration Details
Taiwan FDA Registration: 2d8a6340bdd60ec3aef75b74cea78e26
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Device Details

“Nipro” Disposable Arterial Venous Fistula Set (BioHole, Dull Needle)
TW: “尼普洛”內瘻管翼狀針(鈍針)
Risk Class 2
MD

Registration Details

2d8a6340bdd60ec3aef75b74cea78e26

Ministry of Health Medical Device Import No. 025406

DHA05602540605

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology-urology devices

H5540 Blood access devices and accessories

Imported from abroad

Dates and Status

Sep 10, 2013

Sep 10, 2028