Taiwan FDA registration 02fc972bcda9de9d474df85de845db26

“Philips” IntelliVue Patient Monitor

TW: “飛利浦”病患監視器
Taiwan flagTaiwan·Risk Class 2·MD·PHILIPS MEDIZINSYSTEME BÖBLINGEN GMBH·Registered Nov 19, 2014 – Nov 19, 2024Expired
Registration details
Analysis ID
02fc972bcda9de9d474df85de845db26
License Form
Ministry of Health Medical Device Import No. 026679
Customs Code
DHA05602667906
Company information
Manufacturer Country
Germany
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
Nov 19, 2014
Expiry Date
Nov 19, 2024
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About this record

Access comprehensive regulatory information for “Philips” IntelliVue 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 02fc972bcda9de9d474df85de845db26 and manufactured by PHILIPS MEDIZINSYSTEME BÖBLINGEN GMBH. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including For use only by the Parts System Denda;;For spare parts system only;;Philips Medizin Systeme Böblingen GmbH, 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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