Pure Global
230131
II
current

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This profile provides complete Hong Kong MDACS registration information for Software, Digital Radiographic System, Chest. 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, Digital Radiographic System, Chest

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Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
II
Product Code
26950
Product Code Detail
26950 Software, Digital Radiographic System, Chest
State
current
Status
N/A
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

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Pricing
Manufacturer (่ฃฝ้€ ๅ•†)
GE Medical Systems, LLC
Ge Medical Systems๏ผŒLlc
3000 North Grandview Blvd, Waukesha, WI 53188 UNITED STATES
3000 North Grandview Blvd, ๆฒƒๅŸบๅค, WI 53188 ็พŽๅ›ฝ
Authorised Representative (AR)
21006300
Regulatory Timeline
Registration Date
April 06, 2023
Expiry Date
April 06, 2028
Product Models
Critical Care Suite
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