Taiwan FDA registration 66ec016ef58f8d4aa2e43cfeab7fdf49

Arterial embolization conduit

TW: 動脈栓塞切除導管
Taiwan flagTaiwan·VERMED PHARMACEUTICAL LABORATORY·Registered Jan 29, 1982 – Jan 29, 1987Cancelled
Registration details
Analysis ID
66ec016ef58f8d4aa2e43cfeab7fdf49
Customs Code
DHA00600188403
Company information
Manufacturer Country
France
Authorized Representative
CHINA SPRING TRADING CO., LTD.
Product details
Product Type (Level 1)
0608 Other intensive care units and cardiac intensive care room management
Import Information
import
Dates and status
Registration Date
Jan 29, 1982
Expiry Date
Jan 29, 1987
Cancellation Date
Feb 26, 1990
Cancellation information
Status
Logged out
Reason
有效期限已屆
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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 66ec016ef58f8d4aa2e43cfeab7fdf49 and manufactured by VERMED PHARMACEUTICAL LABORATORY. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including CLINICAL PLASTIC PRODUCTS S.A., DISPO MEDICA GMBH, 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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