Taiwan FDA registration a08b54988ed0ee9bafb87e51ab7f78f4

"Asahi Kosell microcatheter"

TW: “朝日”科塞爾微導管
Taiwan flagTaiwan·Risk Class 2·ASAHI INTECC CO., LTD. SETO FACTORY·Registered Jul 20, 2010 – Jul 20, 2020Cancelled
Registration details
Analysis ID
a08b54988ed0ee9bafb87e51ab7f78f4
Customs Code
DHA00602126401
Company information
Manufacturer Country
Japan
Authorized Representative
QUALTECH CONSULTING CORPORATION
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
Jul 20, 2010
Expiry Date
Jul 20, 2020
Cancellation Date
Jun 07, 2022
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 "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.

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