Taiwan FDA registration fd8176e6e359fd586a392ceecf9d254e

“Teleflex Arrow” Berman Angiographic Balloon Catheters

TW: “泰利福亞諾” 帕曼心血管造影導管

Taiwan·Risk Class 2·MD·Arrow International, LLC (Subsidiary of Teleflex, Incorporated)·Registered Apr 22, 2018 – Apr 22, 2023Expired

Registration details

Analysis ID: fd8176e6e359fd586a392ceecf9d254e
License Form: Ministry of Health Medical Device Import No. 030813
Customs Code: DHA05603081302

Company information

Manufacturer: Arrow International, LLC (Subsidiary of Teleflex, Incorporated)
Manufacturer Country: United States
Authorized Representative: TELEFLEX MEDICAL TAIWAN LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): E Cardiovascular devices
Product Type (Level 2): E1200 Diagnostic endovascular catheter
Import Information: Imported from abroad

Dates and status

Registration Date: Apr 22, 2018
Expiry Date: Apr 22, 2023

About this record

Access comprehensive regulatory information for “Teleflex Arrow” Berman Angiographic Balloon Catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fd8176e6e359fd586a392ceecf9d254e and manufactured by Arrow International, LLC (Subsidiary of Teleflex, Incorporated). The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

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