Taiwan FDA registration 3b0ec9feec542cb3177a56f0e87b2aa6

Central catheter group

TW: 中央導管組
Taiwan flagTaiwan·MAXXIM MEDICAL,ARGON DIVISION·Registered Jul 15, 1991 – Jul 15, 1996Cancelled
Registration details
Analysis ID
3b0ec9feec542cb3177a56f0e87b2aa6
Customs Code
DHA00600639908
Company information
Manufacturer Country
United States
Authorized Representative
Taiwan Bidu Squibb Co., Ltd
Product details
Product Type (Level 1)
1399 Other blood transfusion, infusion equipment
Import Information
import
Dates and status
Registration Date
Jul 15, 1991
Expiry Date
Jul 15, 1996
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 Central catheter group in Taiwan's medical device market through Pure Global AI's free database. is registered under number 3b0ec9feec542cb3177a56f0e87b2aa6 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 ARGON MEDICAL DEVICES, INC., 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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