Taiwan FDA registration 9ef171d8a18619f5782e43e382a9a9c4

"Shengyouda" longitudinal split external guide tube

TW: “聖猷達”縱裂式外導引導管
Taiwan flagTaiwan·Risk Class 2·ST. JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Registered Sep 29, 2007 – Sep 29, 2017Cancelled
Registration details
Analysis ID
9ef171d8a18619f5782e43e382a9a9c4
Customs Code
DHA00601834300
Company information
Manufacturer Country
United States
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.1250 Percutaneous catheters
Import Information
import
Dates and status
Registration Date
Sep 29, 2007
Expiry Date
Sep 29, 2017
Cancellation Date
Nov 04, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Shengyouda" longitudinal split external guide tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9ef171d8a18619f5782e43e382a9a9c4 and manufactured by ST. JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION. The authorized representative in Taiwan is Taiwan Shengyuda Medical Supplies Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ST. JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION;; ST. JUDE MEDICAL, and 1 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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