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CORE Mobile System Medical Equipment
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 400-0100.07
Identity
- Trade Name
- CORE Mobile System Medical Equipment EUDAMEDFDA UDI
- Generic Name
- Cardiovascular ultrasound imaging system FDA UDI
- Device Name
- Core Mobile EUDAMEDCORE Mobile System - 240V FDA UDI
- Model / Reference
- 400-0100.07 EUDAMEDFDA UDI
- Description
- CORE Mobile System - 240V FDA UDI
Identifiers
- Catalog Number
- 400-0100.07 FDA UDI
- Primary DI / UDI-DI
- 00845225012274 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00845225012274 EUDAMED
- 510(k) Number
- K123898 FDA UDI
- FDA Product Code
- IYO FDA UDIDSK FDA UDIDSA FDA UDI
- EMDN Code
- C010499 ANGIOGRAPHY AND HEMODYNAMICS DEVICES - OTHER EUDAMED
- GMDN Term
- Cardiovascular ultrasound imaging system FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 892.1560 FDA UDI870.1110 FDA UDI870.2900 FDA UDI
- Market of Registration
- Belgium EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
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
Yes
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
CORE Mobile System Medical Equipment by Volcano Corporation — Class IIa — 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-00845225012274 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Volcano Corporation
- EUDAMED SRN
- US-MF-000020094
- Authorised Representative
- Volcano Europe BE-AR-000000929
Sources (2)
- EUDAMED 9d42393e-de8f-49f6-be06-5961bd3442ba 61 fields · synced Jun 20, 2026
- FDA UDI 3905475b-778b-4608-baba-6cd185e90a95 36 fields · synced May 29, 2026