Taiwan FDA registration c00d9605fb7494ae0c625247c2125948

Carotid artery diversion duct

TW: 頸動脈分流管
Taiwan flagTaiwan·BAXTER HEALTHCARE CORPORATION, V, MUELLER DIVISION·Registered Aug 01, 1986 – Aug 01, 1991Cancelled
Registration details
Analysis ID
c00d9605fb7494ae0c625247c2125948
Customs Code
DHA00600433702
Company information
Manufacturer Country
United States
Authorized Representative
Blue Line Co., Ltd
Product details
Product Type (Level 1)
0311 Other Artificial Pipes (Manifolds)
Import Information
import
Dates and status
Registration Date
Aug 01, 1986
Expiry Date
Aug 01, 1991
Cancellation Date
Aug 04, 1988
Cancellation information
Status
Logged out
Reason
中文品名變更;;製造廠名稱變更
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About this record

Access comprehensive regulatory information for Carotid artery diversion duct in Taiwan's medical device market through Pure Global AI's free database. is registered under number c00d9605fb7494ae0c625247c2125948 and manufactured by BAXTER HEALTHCARE CORPORATION, V, MUELLER DIVISION. The authorized representative in Taiwan is Blue Line Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including BAXTER HEALTHCARE CORPORATION, V, MUELLER DIVISION, BAXTER RESEARCH MEDICAL INC., 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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