Medical Device Division · registration 180128Active

Coloplast

Name: Coloplast — Medical Device Division 180128
Creator: Coloplast A/S
Keywords: Coloplast, Coloplast, 180128, Procedure Kit/Trays, Implant Delivery, Stent, Ureter, Medical Device Division

Hong KongProcedure Kit/Trays, Implant Delivery, Stent, UreterClass IIIColoplast A/S

Verified

Official record identity

MDACS listing number: 180128
Model name: VORTEK DOUBLE LOOP URETERAL STENT KIT (ACB162, ACB163, ACB164, ACB165, ACB166, ACB167, ACB172, ACB173, ACB174, ACB175, ACB176, ACB177)
Registration date: July 12, 2023
Expiry date: May 12, 2028
Source update date: December 06, 2024
Status: Active

Classification

Risk class: Class III
Published category: Procedure Kit/Trays, Implant Delivery, Stent, Ureter

Published parties

Registrant / registration holder: Keymax Technology (Hong Kong) Ltd.
Manufacturer: Coloplast A/S

Official description

Procedure Kit/Trays, Implant Delivery, Stent, Ureter

Additional source fields

AMD nomenclature code: 17693
Traditional Chinese local responsible person: 啟盈科技 (香港) 有限公司
Local responsible person phone: 31508289
Published manufacturer address: Holtedam 1, 3050 Humlebaek, Denmark
Revision number: b

About this record

This page mirrors one official MDACS listing. Roman-numeral classes use Hong Kong’s general medical-device scheme, while letter classes use the IVD scheme. Valid, expired, and delisted records remain distinguishable; no mixed classification scale is fabricated.