Taiwan FDA registration d2cc585707f1b0850a67280488c59563

"Asahi Uyouke angiography wire"

TW: "朝日"優你客血管造影導線
Taiwan flagTaiwan·Risk Class 2·ASAHI INTECC CO., LTD. SETO FACTORY·Registered Aug 21, 2006 – Aug 21, 2021Cancelled
Registration details
Analysis ID
d2cc585707f1b0850a67280488c59563
Customs Code
DHA00601702402
Company information
Manufacturer Country
Japan
Authorized Representative
QUALTECH CONSULTING CORPORATION
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.1330 Catheter Guide Wires
Import Information
import
Dates and status
Registration Date
Aug 21, 2006
Expiry Date
Aug 21, 2021
Cancellation Date
Sep 08, 2023
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "Asahi Uyouke angiography wire" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d2cc585707f1b0850a67280488c59563 and manufactured by ASAHI INTECC CO., LTD. SETO FACTORY. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including ASAHI INTECC(THAILAND) CO.,LTD, ASAHI INTECC CO., LTD.;; Asahi Intecc Hanoi Co., Ltd., and 2 recent registrations in the same category. 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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