Taiwan FDA registration cdec1d1a05ed6908f197b1e7340ecd8e
Schuma guide tube
TW: 舒瑪導引導管
Registration details
- Analysis ID
- cdec1d1a05ed6908f197b1e7340ecd8e
- Customs Code
- DHA00600918902
Company information
- Manufacturer
- MEDTRONIC VASCULAR
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Medtronic Dingzhong 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
- Jun 07, 1999
- Expiry Date
- Feb 09, 2009
- Cancellation Date
- Nov 06, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Schuma guide tube in Taiwan's medical device market through Pure Global AI's free database. is registered under number cdec1d1a05ed6908f197b1e7340ecd8e and manufactured by MEDTRONIC VASCULAR. The authorized representative in Taiwan is Taiwan Medtronic Dingzhong Co., Ltd.
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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