Taiwan FDA registration 022fdb12aec11df770211051e7c91990

Patient monitors

TW: 病患監護儀
Taiwan flagTaiwan·SIEMENS AG·Registered Jan 29, 1991 – Jan 29, 1996Cancelled
Registration details
Analysis ID
022fdb12aec11df770211051e7c91990
Customs Code
DHA00600618604
Company information
Manufacturer
SIEMENS AG
Manufacturer Country
Germany
Authorized Representative
Schmidt Technology Co., Ltd
Product details
Product Type (Level 1)
0601 Intensive Care Unit and Cardiac Intensive Care Unit Equipment
Import Information
import
Dates and status
Registration Date
Jan 29, 1991
Expiry Date
Jan 29, 1996
Cancellation Date
Dec 13, 2004
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for Patient monitors in Taiwan's medical device market through Pure Global AI's free database. is registered under number 022fdb12aec11df770211051e7c91990 and manufactured by SIEMENS AG. The authorized representative in Taiwan is Schmidt Technology Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KONE OY INSTRUMENT 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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