Pure Global
90082
IV
current

Infusion Pumps输液泵

This profile provides complete Hong Kong MDACS registration information for Infusion Pumps. 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: Infusion Pumps

產品資訊: 输液泵

Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
IV
Product Code
16495
Product Code Detail
16495 Infusion Pumps
State
current
Status
N/A
Pure Global
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DJ Fang

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Manufacturer (製造商)
Medtronic Inc.
Medtronic Plc
United States
美国
710 Medtronic Parkway N.E., Minneapolis MN 55432, USA
710美敦力百汇N.E.,明尼阿波利斯明尼苏达州55432,美国
Authorised Representative (AR)
Regulatory Timeline
Registration Date
October 15, 2024
Expiry Date
April 02, 2029
Product Models
SynchroMed II Programmable Pump (8637-20, 8637-40), Ascenda Intrathecal Catheter (8780, 8781), Ascenda Intrathecal Catheter Spinal Segment Revision Kit (8782), Ascenda Intrathecal Catheter Pump Segment Revision Kit (8784), Ascenda Intrathecal Catheter Accessory Kit (8785), Spinal Needle 9.1 cm (8786), Spinal Needle 15.2cm (8787), Catheter Passer (8583), Catheter Access Port Kit (8540), Refill Kit (8551), Communicator (8880T2), SynchroMed II Clinician Programmer Application (A810)
SynchroMed II 可编程泵 (8637-20, 8637-40), 腾飞鞘内导管 (8780, 8781), 腾飞鞘内导管脊柱节段修订套件 (8782), 腾飞鞘内导管泵分段修订套件 (8784), 腾飞鞘内导管附件套件 (8785), 脊髓针 9.1 cm (8786), 脊髓针 15.2cm (8787), 导管通过器 (8583), 导管接入端口套件 (8540), 补充套件 (8551), 通讯器 (8880T2), 同步医学 II 临床医生编程器应用程序 (A810)