"Asahi Kosell microcatheter"
- Analysis ID
- a08b54988ed0ee9bafb87e51ab7f78f4
- Customs Code
- DHA00602126401
- Manufacturer
- ASAHI INTECC CO., LTD. SETO FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
- 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
- Registration Date
- Jul 20, 2010
- Expiry Date
- Jul 20, 2020
- Cancellation Date
- Jun 07, 2022
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Asahi Kosell microcatheter" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a08b54988ed0ee9bafb87e51ab7f78f4 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, 1 companies making similar products including ASAHI INTECC(THAILAND) CO.,LTD, 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.