240191
III
current
Centralized Patient Monitor集中式患者监护仪
This profile provides complete Hong Kong MDACS registration information for Centralized Patient Monitor. Review device classification, authorised representative (AR) details, manufacturer contacts, product codes, and regulatory milestones. Pure Global AI delivers bilingual transparency for medical device registrations across Asia.
Product Info: Software, Physiologic Monitoring
產品資訊： 软件、生理监测
Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
III
Product Code
26708
Product Code Detail
26708 Software, Physiologic Monitoring
State
current
Status
N/A
Manufacturer (製造商)
Philips Medizin Systeme Böblingen GmbH
Royal Philips
Germany
德国
Hewlett-Packard Strasse 2, 71034 Böblingen, Germany
惠普大街 2, 71034 伯布林根, 德国
Authorised Representative (AR)
28731887 / 28215111/ 26199663
Regulatory Timeline
Registration Date
May 21, 2024
Expiry Date
May 20, 2029
Product Models
Patient Information Center iX (866389, 867093)
患者信息中心 iX (866389, 867093)