90233
IV
Delisted.
Vena cava filter, temporary/permanent่ ้่่ฟๆปคๅจ,ไธดๆถ/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
Delisted.
Status
N/A
Manufacturer (่ฃฝ้ ๅ)
Cordis Europa N.V.
Cordis Europa N.V.
Netherlands
่ทๅ
ฐ
Oosteinde 8, 9301 LJ Roden, Netherlands
Oosteinde 8, 9301 LJ ็ฝ็ป, ่ทๅ
ฐ
Authorised Representative (AR)
Johnson & Johnson (Hong Kong) Limited
ๅผบ็ (้ฆๆธฏ) ๆ้ๅ
ฌๅธ
27386080
Regulatory Timeline
Registration Date
June 23, 2009
Expiry Date
June 23, 2014
Product Models
OptEase Retrievalbe Vena Cava Filter (466-F210A, 466-F210B)
ๅฅฅๆๆฃ็ดข่
้่่ฟๆปคๅจ (466-F210A, 466-F210B)