120435
II
current
Needles, Hemodialysis, Arteriovenous Fistula้ๅคดใ่กๆถฒ้ๆใๅจ้่็
This profile provides complete Hong Kong MDACS registration information for Needles, Hemodialysis, Arteriovenous Fistula. 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: Needles, Hemodialysis, Arteriovenous Fistula
็ขๅ่ณ่จ๏ผ ้ๅคดใ่กๆถฒ้ๆใๅจ้่็
Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
II
Product Code
20230
Product Code Detail
20230 Needles, Hemodialysis, Arteriovenous Fistula
State
current
Status
N/A
Manufacturer (่ฃฝ้ ๅ)
Nipro Corporation
Nipro Corporation
Japan
ๆฅๆฌ
3-9-3, Honjo-Nishi, Kita-ku, Osaka 531-8510, Japan
้ฎ็ผ:531-8510, ๆฅๆฌ ้ฎ็ผ:531-8510, ๅๅบๆฌๅบ่ฅฟ
Authorised Representative (AR)
Baxter Healthcare Ltd.
็พ็นๅป็็จๅๆ้ๅ
ฌๅธ
34053000
Regulatory Timeline
Registration Date
October 17, 2022
Expiry Date
December 31, 2027
Product Models
Fistula Needle (F 15BS G, F 16BS G, F 17BS G, F 15BF G, F 16BF G, F 16BFS G, D-F16BS G, D-F16BSR G)
็็ฎก้ (D 15BS G, F 16BS G, F 17BS G, F 15BF G, F 16BF G, F 16BF G, D-F16BS G, D-F16BSR G)