Carotid artery diversion duct
Taiwan·BAXTER HEALTHCARE CORPORATION, V, MUELLER DIVISION·Registered Jul 25, 1988 – Aug 01, 1991Cancelled- Analysis ID
- b91f39cf41ec7eb16c3a4503233c6af2
- Customs Code
- DHA00600529800
- Manufacturer Country
- United States
- Authorized Representative
- Blue Line Co., Ltd
- Product Type (Level 1)
- 0311 Other Artificial Pipes (Manifolds)
- Import Information
- import
- Registration Date
- Jul 25, 1988
- Expiry Date
- Aug 01, 1991
- Cancellation Date
- Oct 07, 1999
- Status
- Logged out
- Reason
- 改列無須辦理查驗之醫療器材;;未展延而逾期者
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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 b91f39cf41ec7eb16c3a4503233c6af2 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.