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P 3-11

EUDAMED

Class IIa (EU MDR)

Ref 120000001

by Esaote S.p.A.

Identity

Trade Name
P 3-11 EUDAMED
Device Name
P 3-11 EUDAMED
Model / Reference
120000001 EUDAMED

Identifiers

Primary DI / UDI-DI
08056304451309 EUDAMED
Basic UDI-DI
B-08056304451309 EUDAMED
EMDN Code
Z110402010301 TRANSCUTANEOUS ULTRASOUND SECTOR PROBES (PHASED ARRAY), TWO–DIMENSIONAL EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

P 3-11 by Esaote S.p.A. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Esaote S.p.A.
EUDAMED SRN
IT-MF-000019024

Sources (1)

  • EUDAMED dfc270fc-a425-4917-82b7-368df94ba95f 61 fields · synced Jul 10, 2026