Medical Device Division · registration 090233CancelledCordis
Hong KongVena cava filter, temporary/permanentClass IVCordis Europa N.V.
Official record identity
- MDACS listing number
- 090233
- Model name
- OptEase Retrievalbe Vena Cava Filter (466-F210A, 466-F210B)
- Registration date
- June 23, 2009
- Source update date
- July 15, 2025
- Status
- Cancelled
Official value: Delisted
Classification
- Risk class
- Class IV
Official value: IV
Published parties
- Registrant / registration holder
- Johnson & Johnson (Hong Kong) Limited
- Manufacturer
- Cordis Europa N.V.
Additional source fields
- Traditional Chinese local responsible person
- 強生 (香港) 有限公司
- Local responsible person phone
- 27386080
- Published manufacturer address
- Oosteinde 8, 9301 LJ Roden, Netherlands
- Published remarks
- Delisted.
- Revision number
- b
- Delist date
- 2016-10-25
About this record
This page mirrors one official MDACS listing. Roman-numeral classes use Hong Kong’s general medical-device scheme, while letter classes use the IVD scheme. Valid, expired, and delisted records remain distinguishable; no mixed classification scale is fabricated.