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"Nipro" Pholast balloon dilation catheter - Taiwan Registration 8156e48be85e269b3cfac9d8664894c8

Access comprehensive regulatory information for "Nipro" Pholast balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8156e48be85e269b3cfac9d8664894c8 and manufactured by Goodman Co., Ltd. Goodman Research Center;; Goodman Co., Ltd.. The authorized representative in Taiwan is HORNG FWU PHARMA CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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8156e48be85e269b3cfac9d8664894c8
Registration Details
Taiwan FDA Registration: 8156e48be85e269b3cfac9d8664894c8
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Device Details

"Nipro" Pholast balloon dilation catheter
TW: โ€œๅฐผๆ™ฎๆด›โ€ๆฑŽๅธ็‰น็ƒๅ›Šๆ“ดๅผตๅฐŽ็ฎก
Risk Class 2

Registration Details

8156e48be85e269b3cfac9d8664894c8

DHA05603606809

Company Information

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Dec 18, 2022

Dec 18, 2027