090233
Vena cava filter, temporary/permanent
下腔静脉滤器，临时/永久
Cordis Europa N.V.·IV·Hong Kong MDACS·Registered June 23, 2009Delisted
Device overview
- Risk class
- IV
- Product code
- N/A
- State
- N/A
- Status
- Delisted已退市
Manufacturer (製造商)
- Name
- Cordis Europa N.V.Cordis Europa N.V.
- Country
- Netherlands荷兰
- Address
- Oosteinde 8, 9301 LJ Roden, Netherlands荷兰罗登市Oosteinde 8, 9301 LJ
Authorised representative (AR)
- Name
- Johnson & Johnson (Hong Kong) Limited强生 (香港) 有限公司
- Phone
- 27386080
Regulatory timeline
- Registration date
- June 23, 2009
- Expiry date
- June 23, 2014
- Delist date
- October 25, 2016
Product models
OptEase Retrievalbe Vena Cava Filter (466-F210A, 466-F210B)
Remarks
Delisted.
已從列表中刪除。
About this record
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.