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Ampraz Twilip catheter - Taiwan Registration 79dfe821342b6daf0359b1690c58a7b0

Access comprehensive regulatory information for Ampraz Twilip catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 79dfe821342b6daf0359b1690c58a7b0 and manufactured by AGA MEDICAL CORPORATION. The authorized representative in Taiwan is Taiwan Shengyuda Medical Supplies 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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79dfe821342b6daf0359b1690c58a7b0
Registration Details
Taiwan FDA Registration: 79dfe821342b6daf0359b1690c58a7b0
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Device Details

Ampraz Twilip catheter
TW: ๅฎ‰ๆ™ฎๆ‹‰่Œฒ็‰น็ถญๅŠ›ๆ™ฎๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

79dfe821342b6daf0359b1690c58a7b0

DHA00602391408

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Jul 31, 2012

Jul 31, 2017

Nov 04, 2019

Cancellation Information

Logged out

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