230373
III
current
Radiographic/Fluoroscopic Systems, Angiography/Interventionalๆพๅฐ/้่ง็ณป็ป,่ก็ฎก้ ๅฝฑ/ไปๅ ฅ
This profile provides complete Hong Kong MDACS registration information for Radiographic/Fluoroscopic Systems, Angiography/Interventional. 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: Radiographic/Fluoroscopic Systems, Angiography/Interventional
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Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
III
Product Code
16597
Product Code Detail
16597 Radiographic/Fluoroscopic Systems, Angiography/Interventional
State
current
Status
N/A
Brand
Philips
้ฃๅฉๆตฆ
Manufacturer (่ฃฝ้ ๅ)
Philips Medical Systems Nederland B.V.
Philips Medical Systems Nederland B.V.
Netherlands
่ทๅ
ฐ
Veenpluis 6
5684 PC Best
The Netherlands
็ปดๆฉๆฎ้ฒๆฏ 6
5684 PC ๆไฝณ
่ทๅ
ฐ
Authorised Representative (AR)
28731887 / 28215111/ 26199663
Regulatory Timeline
Registration Date
October 19, 2023
Expiry Date
October 19, 2028
Product Models
Azurion 3 M12 (722 221), Azurion 3 M15 (722 222), Azurion 5 M12 (722 227), Azurion 5 M20 (722 228), Azurion 7 M12 (722 223), Azurion 7 M20 (722 224), Azurion 7 B12 (722 225), Azurion 7 B20 (722 226)
่็ 3 M12 (722,221), ่็ 3 M15 (722,222), ่็ 5 M12 (722,227), ่็ 5 M20 (722,228), ่็ 7 M12 (722,223), ่็ 7 M20 (722,224), ่็ 7,B12 (722,225), ่็ 7,B20 (722,226)