090232
Angioplasty catheter, balloon dilatation, peripheral
血管成形导管，球囊扩张，外周
Cordis Europa N.V.·II·Hong Kong MDACS·Registered June 23, 2009Delisted
Device overview
- Risk class
- II
- Product code
- 17184
- 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
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)
Remarks
Delisted.
已從列表中刪除。
About this record
This profile provides complete Hong Kong MDACS registration information for Angioplasty catheter, balloon dilatation, peripheral. 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.
Product Info: Catheters, Vascular, Angioplasty, Balloon
產品資訊： 导管、血管、血管成形术、球囊