Taiwan FDA registration 13007bec2eb062c170fa026c855d6669

Perimeter guide tube

TW: 周邊導引導管
Taiwan flagTaiwan·CORDIS CORPORATION·Registered May 10, 2000 – May 10, 2005Cancelled
Registration details
Analysis ID
13007bec2eb062c170fa026c855d6669
Customs Code
DHA00600940900
Company information
Manufacturer
CORDIS CORPORATION
Manufacturer Country
United States
Product details
Product Type (Level 1)
0699 Other Intensive Care Unit & Cardiac Care Unit Equipment
Import Information
import
Dates and status
Registration Date
May 10, 2000
Expiry Date
May 10, 2005
Cancellation Date
Nov 27, 2012
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for Perimeter guide tube in Taiwan's medical device market through Pure Global AI's free database. is registered under number 13007bec2eb062c170fa026c855d6669 and manufactured by CORDIS CORPORATION. The authorized representative in Taiwan is Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch.

This page provides complete technical specifications, regulatory compliance details. 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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