180128
III
current
Procedure Kit/Trays, Implant Delivery, Stent, Ureterๆๆฏๅฅไปถ/ๆ็, ๆคๅ ฅ็ฉ่พ้, ๆฏๆถ, ่พๅฐฟ็ฎก
This profile provides complete Hong Kong MDACS registration information for Procedure Kit/Trays, Implant Delivery, Stent, Ureter. 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: Procedure Kit/Trays, Implant Delivery, Stent, Ureter
็ขๅ่ณ่จ๏ผ ๆๆฏๅฅไปถ/ๆ็, ๆคๅ ฅ็ฉ่พ้, ๆฏๆถ, ่พๅฐฟ็ฎก
Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
III
Product Code
17693
Product Code Detail
17693 Procedure Kit/Trays, Implant Delivery, Stent, Ureter
State
current
Status
N/A
Brand
Vortek
ๆฒๆณฐๅ
Manufacturer (่ฃฝ้ ๅ)
Coloplast A/S
Coloplast
Denmark
ไธน้บฆ
Holtedam 1, 3050 Humlebaek, Denmark
Holtedam 1, 3050 ่กๅงๅๆๅ
, ไธน้บฆ
Authorised Representative (AR)
Keymax Technology (Hong Kong) Ltd.
ๅฏ็็งๆ (้ฆๆธฏ) ๆ้ๅ
ฌๅธ
31508289
Regulatory Timeline
Registration Date
July 12, 2023
Expiry Date
May 12, 2028
Product Models
VORTEK DOUBLE LOOP URETERAL STENT KIT (ACB162, ACB163, ACB164, ACB165, ACB166, ACB167, ACB172, ACB173, ACB174, ACB175, ACB176, ACB177)
VORTEK ๅ่ขข่พๅฐฟ็ฎกๆฏๆถๅฅไปถ (ACB162, ACB163, ACB164, ACB165, ACB166, ACB167, ACB172, ACB173, ACB174, ACB175, ACB176, ACB177)