Medical Device Division · registration 090232CancelledCordis
Hong KongAngioplasty catheter, balloon dilatation, peripheralClass IICordis Europa N.V.
Official record identity
- MDACS listing number
- 090232
- Model name
- Maxi LD PTA Dilatation Catheter (4161440V, 4161440S, 4161440L, 4161440X, 4161460V, 4161460S, 4161460L, 4161460X, 4161520VF, 4161520SF, 4161520LF, 4161520X, 4161540VF, 4161540S, 4161540L, 4161540X, 4161560VF, 4161560S, 4161560L, 4161560X, 4161640V, 4161640S, 4161640L, 4161640X, 4161660V, 4161660S, 4161660L, 4161660X, 4161840V, 4161840S, 4161840L, 4161840X, 4161860V, 4161860S, 4161860L, 4161860X, 4162040VF, 4162040S, 4162040L, 4162040X, 4162060VF, 4162060S, 4162060L, 4162060X, 4162080VF, 4162080S, 4162080L, 4162080X, 4162240L, 4162240S, 4162440V, 4162440S, 4162440L, 4162440X, 4162540VF, 4162540S, 4162540L, 4162540X)
- Registration date
- June 23, 2009
- Source update date
- July 15, 2025
- Status
- Cancelled
Official value: Delisted
Classification
- Risk class
- Class II
Official value: II
Published parties
- Registrant / registration holder
- Johnson & Johnson (Hong Kong) Limited
- Manufacturer
- Cordis Europa N.V.
Official description
Catheters, Vascular, Angioplasty, Balloon
Additional source fields
- AMD nomenclature code
- 17184
- 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.