090292
III
Delisted
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This profile provides complete Hong Kong MDACS registration information for Stents, Vascular, Renal Artery. 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: Stents, Vascular, Renal Artery
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Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
III
Product Code
20428
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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Oosteinde 8, 9301 LJ Roden, Netherlands
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Authorised Representative (AR)
Johnson & Johnson (Hong Kong) Limited
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27386080
Regulatory Timeline
Registration Date
July 27, 2009
Expiry Date
July 27, 2014
Delist Date
October 25, 2016
Remarks
Delisted.
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Product Models
PALMAZ BLUE .014 Peripheral Stent System