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Applicant profile

Cordis Europa N.V.

Cordis Europa N.V.
Hong Kong MDACSNetherlands27 registered devicesJun 16, 2005 – Jan 13, 2010
VerifiedMDD (Medical Device Division) · MDACS registry
27
Total devices
3
Risk classes
2005
First registration
2010
Most recent
Applicant overview
Applicant (EN)
Cordis Europa N.V.
Applicant (ZH)
Cordis Europa N.V.
Country
Netherlands
荷兰
Address
Oosteinde 8, 9301 LJ Roden, Netherlands
荷兰罗登，9301 LJ，Oosteinde 8号
Timeline
First registration
Jun 16, 2005
Most recent
Jan 13, 2010
Regulatory footprint
Search Cordis Europa N.V. across other regulatory registries
ThailandEuropean UnionColombiaSouth KoreaCanadaEcuador
Risk class breakdown
II6
III7
IV14
Recent MDACS registrations
Latest 15 devices linked to this applicant
Stents, Vascular, Peripheral
外周血管支架
Jan 13, 2010
Risk class
III
Authorised rep
Johnson & Johnson (Hong Kong) Limited强生 (香港) 有限公司
Stents, Vascular, Peripheral
支架,血管,外周
Nov 04, 2009
Risk class
III
Authorised rep
Johnson & Johnson (Hong Kong) Limited强生 (香港) 有限公司
Stents, Vascular, Peripheral
外周血管支架
Nov 04, 2009
Risk class
III
Authorised rep
Johnson & Johnson (Hong Kong) Limited强生 (香港) 有限公司
Catheters, Vascular, Angioplasty, Balloon
导管、血管、血管成形术、球囊
Sep 02, 2009
Risk class
II
Authorised rep
Johnson & Johnson (Hong Kong) Limited强生 (香港) 有限公司
Catheters, Vascular, Angioplasty, Balloon
导管、血管、血管成形术、球囊
Sep 02, 2009
Risk class
II
Authorised rep
Johnson & Johnson (Hong Kong) Limited强生 (香港) 有限公司
Stents, Vascular, Renal Artery
支架、血管、肾动脉
Jul 27, 2009
Risk class
III
Authorised rep
Johnson & Johnson (Hong Kong) Limited强生 (香港) 有限公司
Stents, Vascular, Renal Artery
支架、血管、肾动脉
Jul 27, 2009
Risk class
III
Authorised rep
Johnson & Johnson (Hong Kong) Limited强生 (香港) 有限公司
Stent/Grafts, Vascular, Peripheral
支架/移植物，血管，外周
Jul 27, 2009
Risk class
III
Authorised rep
Johnson & Johnson (Hong Kong) Limited强生 (香港) 有限公司
Stent/Grafts, Vascular, Peripheral
支架/移植物,血管,外周
Jul 27, 2009
Risk class
III
Authorised rep
Johnson & Johnson (Hong Kong) Limited强生 (香港) 有限公司
Angioplasty catheter, balloon dilatation, peripheral
血管成形导管，球囊扩张，外周
Jun 23, 2009
Risk class
II
Authorised rep
Johnson & Johnson (Hong Kong) Limited强生 (香港) 有限公司
Angioplasty catheter, balloon dilatation, peripheral
血管成形导管，球囊扩张，外周
Jun 23, 2009
Risk class
II
Authorised rep
Johnson & Johnson (Hong Kong) Limited强生 (香港) 有限公司
Vena cava filter, temporary/permanent
下腔静脉滤器，临时/永久
Jun 23, 2009
Risk class
IV
Authorised rep
Johnson & Johnson (Hong Kong) Limited强生 (香港) 有限公司
Vena cava filter, temporary/permanent
腔静脉过滤器,临时/永久
Jun 23, 2009
Risk class
IV
Authorised rep
Johnson & Johnson (Hong Kong) Limited强生 (香港) 有限公司
Angioplasty catheter, balloon dilatation, peripheral
血管成形术导管、球囊扩张术、外周
Jun 23, 2009
Risk class
II
Authorised rep
Johnson & Johnson (Hong Kong) Limited强生 (香港) 有限公司
Angioplasty catheter, balloon dilatation, peripheral
血管成形术导管、球囊扩张术、外周
Jun 23, 2009
Risk class
II
Authorised rep
Johnson & Johnson (Hong Kong) Limited强生 (香港) 有限公司
View all 27 devices →
About this profile

Cordis Europa N.V. is associated with 27 medical devices registered under the Hong Kong Medical Device Administrative Control System (MDACS). Explore bilingual product names, risk classes, authorised representatives, and life-cycle milestones.