Taiwan FDA registration f30c5d327e3e6b18a118895789df59e1

"Philips" patient monitor

TW: "飛利浦"病患監視器
Taiwan flagTaiwan·Risk Class 2·PHILIPS MEDIZINSYSTEME BUBBLE GMBH;; 台灣飛利浦股份有限公司·Registered Nov 26, 2009 – Feb 09, 2029Active
Registration details
Analysis ID
f30c5d327e3e6b18a118895789df59e1
Customs Code
DHA00600800306
Company information
Manufacturer Country
Taiwan, Province of China;;Germany
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
Vacuum.
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.1025 Arrhythmia Detectors and Alerts
Import Information
import
Dates and status
Registration Date
Nov 26, 2009
Expiry Date
Feb 09, 2029
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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 f30c5d327e3e6b18a118895789df59e1 and manufactured by PHILIPS MEDIZINSYSTEME BUBBLE GMBH;; 台灣飛利浦股份有限公司. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including PHILIPS MEDIZINSYSTEME BÖBLINGEN GMBH, PHILIPS MEDICAL SYSTEMS, and 5 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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