090233
IV
Delisted
Vena cava filter, temporary/permanentไธ่ ้่ๆปคๅจ๏ผไธดๆถ/ๆฐธไน
This profile provides complete Hong Kong MDACS registration information for Vena cava filter, temporary/permanent. 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.
Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
IV
Product Code
N/A
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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ฐ็ฝ็ปๅธOosteinde 8, 9301 LJ
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
OptEase Retrievalbe Vena Cava Filter (466-F210A, 466-F210B)