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s5i

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 807400001

by Volcano Corporation

Identity

Trade Name
s5i EUDAMED
s5i Imaging System FDA UDI
Generic Name
Cardiovascular ultrasound imaging system FDA UDI
Device Name
s5i EUDAMED
Model / Reference
807400001 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
00845225010218 EUDAMEDFDA UDI
Basic UDI-DI
B-00845225010218 EUDAMED
510(k) Number
K071554 FDA UDI
FDA Product Code
IYO FDA UDI
OBJ FDA UDI
EMDN Code
C010499 ANGIOGRAPHY AND HEMODYNAMICS DEVICES - OTHER EUDAMED
GMDN Term
Cardiovascular ultrasound imaging system FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
892.1560 FDA UDI
870.1200 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

s5i 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

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Manufacturer

Manufacturer
Volcano Corporation
EUDAMED SRN
US-MF-000020094
Authorised Representative
Volcano Europe BE-AR-000000929

Sources (2)

  • EUDAMED b3c6aa59-2612-437f-bf0b-dbb109176fa9 61 fields · synced Jul 18, 2026
  • FDA UDI be7c690b-2c2c-4224-8bb7-9ef6624358ea 33 fields · synced May 30, 2026