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Reperfusion Catheter 3MAX, 153 cm
EUDAMEDFDA UDIClass III (EU MDR)
Ref 3MAXCModel Reperfusion Catheter
Identity
- Trade Name
- Reperfusion Catheter 3MAX, 153 cm EUDAMEDPenumbra System FDA UDI
- Generic Name
- Thrombectomy suction catheter FDA UDI
- Device Name
- Penumbra System EUDAMEDPS MAX RC3MAX FDA UDI
- Model / Reference
- Reperfusion Catheter EUDAMED3MAXC EUDAMEDFDA UDI
- Description
- PS MAX RC3MAX FDA UDI
Identifiers
- Primary DI / UDI-DI
- D-PenumbraSystem94 EUDAMED00814548012490 FDA UDI
- Basic UDI-DI
- B-PenumbraSystem94 EUDAMED
- 510(k) Number
- K113163 FDA UDI
- FDA Product Code
- NRY FDA UDI
- EMDN Code
- C010402020702 MECHANICAL PERIPHERAL THROMBECTOMY AND THROMBOASPIRATION SYSTEMS EUDAMED
- GMDN Term
- Thrombectomy suction catheter FDA UDI
Classification
- Device Class
- Class III EUDAMEDClass II FDA UDI
- Regulation Number
- 870.1250 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Reperfusion Catheter 3MAX, 153 cm by Penumbra, Inc. — Class III — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-PenumbraSystem94 | Class III | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
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Manufacturer
- Manufacturer
- Penumbra, Inc.
- EUDAMED SRN
- US-MF-000008514
- Authorised Representative
- Penumbra Europe GmbH DE-AR-000004997
Sources (2)
- EUDAMED 283a9907-d8ae-4248-b93f-af9f50eda858 61 fields · synced Jul 19, 2026
- FDA UDI fe6fd40c-7176-4966-aa35-51ae5ef9fe61 34 fields · synced May 27, 2026