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Applicant profile

Penumbra, Inc.

Penumbra,Inc.
Hong Kong MDACSUnited States10 registered devicesMar 28, 2013 – Oct 16, 2024
VerifiedMDD (Medical Device Division) · MDACS registry
10
Total devices
2
Risk classes
2013
First registration
2024
Most recent
Applicant overview
Applicant (EN)
Penumbra, Inc.
Applicant (ZH)
Penumbra,Inc.
Country
United States
美国
Brand
INDIGO
靛
Address
One Penumbra Place, Alameda, CA 94502, USA
半影广场一号,阿拉米达,CA 94502,美国
Timeline
First registration
Mar 28, 2013
Most recent
Oct 16, 2024
Regulatory footprint
Search Penumbra, Inc. across other regulatory registries
ThailandEuropean UnionColombiaSouth KoreaCanadaEcuador
Risk class breakdown
II1
IV9
Recent MDACS registrations
Latest 15 devices linked to this applicant
Catheters, Vascular, Embolectomy/Thrombectomy
导管、血管、栓塞切除术/血栓切除术
Oct 16, 2024
Risk class
IV
Authorised rep
Asia Actual Limited
Catheters, Vascular, Embolectomy/Thrombectomy
导管、血管、栓塞切除术/血栓切除术
Jul 24, 2024
Risk class
IV
Authorised rep
Asia Actual Limited
Catheters, Vascular, Microflow
导管,血管,微流
Jun 06, 2024
Risk class
IV
Authorised rep
Asia Actual Limited
Catheters, Vascular, Guiding
导管,血管,引导
Nov 27, 2023
Risk class
IV
Authorised rep
Asia Actual Limited
Aspirators, Surgical
吸引器,外科
Nov 18, 2020
Risk class
II
Authorised rep
Asia Actual Limited
Occluders, Vascular, Intravascular Embolization, Coil
封堵器,血管,血管内栓塞,线圈
Jul 02, 2020
Risk class
IV
Authorised rep
Synapse Therapeutics Limited百谷医疗科技有限公司
Occluders, Vascular, Intravascular Embolization, Coil
封堵器,血管,血管内栓塞,线圈
Mar 28, 2018
Risk class
IV
Authorised rep
Synapse Therapeutics Limited百谷医疗科技有限公司
Catheters, Vascular, Guiding
导管,血管,引导
Jan 18, 2016
Risk class
IV
Authorised rep
Synapse Therapeutics Limited百谷医疗科技有限公司
Catheters, Vascular, Embolectomy/Thrombectomy
导管、血管、栓塞切除术/血栓切除术
Jan 18, 2016
Risk class
IV
Authorised rep
Synapse Therapeutics Limited百谷医疗科技有限公司
Catheters, Intracranial
颅内导管
Mar 28, 2013
Risk class
IV
Authorised rep
Synapse Therapeutics Limited百谷医疗科技有限公司
About this profile

Penumbra, Inc. is associated with 10 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.