Taiwan FDA registration f3c8ba48bf8c3fb317e58abb8d39beb4

Platyfenda angiography catheter

TW: 柏芬達血管攝影導管
Taiwan flagTaiwan·MAXXIM MEDICAL,ARGON DIVISION·Registered Feb 13, 1989 – Feb 13, 1994Cancelled
Registration details
Analysis ID
f3c8ba48bf8c3fb317e58abb8d39beb4
Customs Code
DHA00600548305
Company information
Manufacturer Country
United States
Authorized Representative
Taiwan Bidu Squibb Co., Ltd
Product details
Product Type (Level 1)
0699 Other Intensive Care Unit & Cardiac Care Unit Equipment
Import Information
import
Dates and status
Registration Date
Feb 13, 1989
Expiry Date
Feb 13, 1994
Cancellation Date
Jan 22, 1994
Cancellation information
Status
Logged out
Reason
移轉(申請商)
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About this record

Access comprehensive regulatory information for Platyfenda angiography catheter in Taiwan's medical device market through Pure Global AI's free database. is registered under number f3c8ba48bf8c3fb317e58abb8d39beb4 and manufactured by MAXXIM MEDICAL,ARGON DIVISION. The authorized representative in Taiwan is Taiwan Bidu Squibb Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MAXXIM MEDICAL,ARGON DIVISION, 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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