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Kosmos Bridge

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref P006030

by EchoNous

Identity

Trade Name
Kosmos Bridge EUDAMEDFDA UDI
Generic Name
Ultrasound/electrocardiograph/stethoscope unit FDA UDI
Device Name
Kosmos EUDAMED
Diagnostic ultrasound system with integrated electronic stethoscope and electrocardiograph Ultrasound/ electrocardiograph/ stethoscope unit FDA UDI
Model / Reference
P006030 EUDAMEDFDA UDI
Description
Diagnostic ultrasound system with integrated electronic stethoscope and electrocardiograph Ultrasound/ electrocardiograph/ stethoscope unit FDA UDI

Identifiers

Primary DI / UDI-DI
09353278000120 EUDAMEDFDA UDI
Basic UDI-DI
93532780KOSMOSWH EUDAMED
510(k) Number
K193518 FDA UDI
FDA Product Code
IYO FDA UDI
IYN FDA UDI
DQD FDA UDI
DPS FDA UDI
EMDN Code
Z11040106 HANDHELD ULTRASOUND SCANNERS EUDAMED
GMDN Term
Ultrasound/electrocardiograph/stethoscope unit FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
892.1560 FDA UDI
892.1550 FDA UDI
870.1875 FDA UDI
870.2340 FDA UDI
Market of Registration
Malta 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

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

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

Kosmos Bridge by EchoNous — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
EchoNous
EUDAMED SRN
US-MF-000004161
Authorised Representative
Advena Limited MT-AR-000000234

Sources (2)

  • EUDAMED 4e34437c-a5ea-4abe-be9b-c3380b20cbf5 61 fields · synced Jul 19, 2026
  • FDA UDI 888d613d-f11f-44f3-b846-c427fbe42888 34 fields · synced May 30, 2026