120435
Needles, Hemodialysis, Arteriovenous Fistula
针头、血液透析、动静脉瘘
Nipro Corporation·II·Hong Kong MDACS·Registered October 17, 2022
Device overview
- Risk class
- II
- Product code
- 20230
- State
- current
- Status
- N/A
- Product code detail
- 20230 Needles, Hemodialysis, Arteriovenous Fistula
Manufacturer (製造商)
- Name
- Nipro CorporationNipro Corporation
- Country
- Japan日本
- Address
- 3-9-3, Honjo-Nishi, Kita-ku, Osaka 531-8510, Japan邮编:531-8510, 日本 邮编:531-8510, 北区本庄西
Authorised representative (AR)
- Name
- Baxter Healthcare Ltd.百特医疗用品有限公司
- Phone
- 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)
瘘管针 (D 15BS G, F 16BS G, F 17BS G, F 15BF G, F 16BF G, F 16BF G, D-F16BS G, D-F16BSR G)
About this record
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
產品資訊： 针头、血液透析、动静脉瘘