090232
II
Delisted
Angioplasty catheter, balloon dilatation, peripheral่ก็ฎกๆๅฝขๅฏผ็ฎก๏ผ็ๅๆฉๅผ ๏ผๅคๅจ
This profile provides complete Hong Kong MDACS registration information for Angioplasty catheter, balloon dilatation, peripheral. 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: Catheters, Vascular, Angioplasty, Balloon
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Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
II
Product Code
17184
State
N/A
Status
Delisted
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Manufacturer (่ฃฝ้ ๅ)
Cordis Europa N.V.
Cordis Europa N.V.
Netherlands
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ฐ
Oosteinde 8, 9301 LJ Roden, Netherlands
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Authorised Representative (AR)
Johnson & Johnson (Hong Kong) Limited
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ฌๅธ
27386080
Regulatory Timeline
Registration Date
June 23, 2009
Expiry Date
June 23, 2014
Delist Date
October 25, 2016
Remarks
Delisted.
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Product Models
Maxi LD PTA Dilatation Catheter (4161440V, 4161440S, 4161440L, 4161440X, 4161460V, 4161460S, 4161460L, 4161460X, 4161520VF, 4161520SF, 4161520LF, 4161520X, 4161540VF, 4161540S, 4161540L, 4161540X, 4161560VF, 4161560S, 4161560L, 4161560X, 4161640V, 4161640S, 4161640L, 4161640X, 4161660V, 4161660S, 4161660L, 4161660X, 4161840V, 4161840S, 4161840L, 4161840X, 4161860V, 4161860S, 4161860L, 4161860X, 4162040VF, 4162040S, 4162040L, 4162040X, 4162060VF, 4162060S, 4162060L, 4162060X, 4162080VF, 4162080S, 4162080L, 4162080X, 4162240L, 4162240S, 4162440V, 4162440S, 4162440L, 4162440X, 4162540VF, 4162540S, 4162540L, 4162540X)