70113
Catheter, angioplasty, balloon dilatation
导管、血管成形术、球囊扩张术
OrbusNeich Medical B.V.·IV·Hong Kong MDACS·Registered October 29, 2007
Device overview
- Risk class
- IV
- Product code
- N/A
- State
- Expired.
- Status
- N/A
Manufacturer (製造商)
- Name
- OrbusNeich Medical B.V.Orbusneich Medical, B.V.
Authorised representative (AR)
- Name
- OrbusNeich Medical Company Limited业聚医疗有限公司
- Phone
- 31097271/31097216
Regulatory timeline
- Registration date
- October 29, 2007
- Expiry date
- October 29, 2012
Product models
Sapphire Coronary Dilatation Catheter (103-1205, 103-1208, 103-1210, 103-1215, 103-1510, 103-1515, 103-1520, 103-2010, 103-2015, 103-2020, 103-2210, 103-2215, 103-2220, 103-2510, 103-2515, 103-2520, 103-2530, 103-2710, 103-2715, 103-2720, 103-3010, 103-3015, 103-3020, 103-3030, 103-3210, 103-3215, 103-3220, 103-3510, 103-3515, 103-3520, 103-3530, 103-4010, 103-4015, 103-4020)
蓝宝石冠状动脉扩张导管 (103-1205, 103-1208, 103-1210, 103-1215, 103-1510, 103-1515, 103-1520, 103-2010, 103-2015, 103-2020, 103-2210, 103-2215, 103-2220, 103-2510, 103-2515, 103-2520, 103 -2530, 103-2710, 103-2715, 103-2720, 103-3010, 103-3015, 103-3020, 103-3030, 103-3210, 103-3215, 103-3220, 103-3510, 103-3515, 103-3520, 103-3530, 103-4010, 103-4015, 103-4020)
About this record
This profile provides complete Hong Kong MDACS registration information for Catheter, angioplasty, balloon dilatation. 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.