Taiwan FDA registration b8f768b788031727cccb54007ecbb171

“Philips” Patient Monitor

TW: “飛利浦”病患監視器
Taiwan flagTaiwan·Risk Class 2·MD·PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH;;For use only by the Parts System Denda;;For spare parts system only·Registered Sep 22, 2020 – Sep 22, 2025Expired
Registration details
Analysis ID
b8f768b788031727cccb54007ecbb171
License Form
Ministry of Health Medical Device Import No. 033960
Customs Code
DHA05603396001
Company information
Manufacturer Country
China;;United States;;Germany;;Austria
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular devices
Product Type (Level 2)
E1025 Arrhythmia detector and alert
Import Information
Imported from abroad
Dates and status
Registration Date
Sep 22, 2020
Expiry Date
Sep 22, 2025
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About this record

Access comprehensive regulatory information for “Philips” Patient Monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b8f768b788031727cccb54007ecbb171 and manufactured by PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH;;For use only by the Parts System Denda;;For spare parts system only. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH;;For use only by the Parts System Denda;;For spare parts system only, For spare parts system only;;PHILIPS MEDICAL SYSTEMS BOEBLINGEN GMBH, and 2 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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