Taiwan FDA registration 505de69445e5663e26a8955b1ffe04e9

"Philips" Central Monitoring Station software

TW: “飛利浦” 中央監視站軟體
Taiwan flagTaiwan·Risk Class 2·Philips Medizin Systeme Böblingen GmbH;; Philips North America LLC·Registered Mar 29, 2024 – Mar 29, 2029Active
Registration details
Analysis ID
505de69445e5663e26a8955b1ffe04e9
Customs Code
DHA05603695204
Company information
Manufacturer Country
United States;;Germany
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
Details are as detailed as approved Chinese instructions
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
Mar 29, 2024
Expiry Date
Mar 29, 2029
About this record

Access comprehensive regulatory information for "Philips" Central Monitoring Station software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 505de69445e5663e26a8955b1ffe04e9 and manufactured by Philips Medizin Systeme Böblingen GmbH;; Philips North America LLC. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details. 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.

Free DatabasePowered by Pure Global AI89,000+ Devices