Taiwan FDA registration 377ce9ab0e5fa6cfa816d5bfd7c917de

“Philips” IntelliVue Information Center iX

TW: “飛利浦”中央監視站軟體
Taiwan flagTaiwan·Risk Class 2·MD·PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH·Registered Dec 19, 2019 – Dec 19, 2024Expired
Registration details
Analysis ID
377ce9ab0e5fa6cfa816d5bfd7c917de
License Form
Ministry of Health Medical Device Import No. 033071
Customs Code
DHA05603307109
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
Dec 19, 2019
Expiry Date
Dec 19, 2024
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About this record

Access comprehensive regulatory information for “Philips” IntelliVue Information Center iX in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 377ce9ab0e5fa6cfa816d5bfd7c917de and manufactured by PHILIPS MEDIZIN SYSTEME BOEBLINGEN 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 PHILIPS MEDICAL SYSTEMS, 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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