Taiwan FDA registration f64c62be4fec46e218f265e2f528108f

Arterial embolization conduit

TW: 動脈栓塞切除導管
Taiwan flagTaiwan·AMERICAN BIOMED, INCORPORATED-CATHLAB DIVISION·Registered May 20, 1994 – May 20, 1999Cancelled
Registration details
Analysis ID
f64c62be4fec46e218f265e2f528108f
Customs Code
DHA00600721200
Company information
Manufacturer Country
United States
Product details
Intended Use
The details are as detailed as the approved copy of the imitation label
Product Type (Level 1)
0699 Other Intensive Care Unit & Cardiac Care Unit Equipment
Import Information
import
Dates and status
Registration Date
May 20, 1994
Expiry Date
May 20, 1999
Cancellation Date
Aug 30, 2007
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 Arterial embolization conduit in Taiwan's medical device market through Pure Global AI's free database. is registered under number f64c62be4fec46e218f265e2f528108f and manufactured by AMERICAN BIOMED, INCORPORATED-CATHLAB DIVISION. The authorized representative in Taiwan is Swiss company Keith & Co., Ltd. Taipei Branch.

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including VERMED PHARMACEUTICAL LABORATORY, CLINICAL PLASTIC PRODUCTS S.A., and 3 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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