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Px 4-13

EUDAMED

Class IIa (EU MDR)

Ref 120000207

by Esaote S.p.A.

Identity

Trade Name
PX 4-13 EUDAMED
Device Name
Phased Array / High and Ultra High Frequency EUDAMED
Model / Reference
120000207 EUDAMED

Identifiers

Primary DI / UDI-DI
08056304456229 EUDAMED
Basic UDI-DI
805630445ESA.PR0000013.SW EUDAMED
EMDN Code
Z110402010302 TRANSCUTANEOUS ULTRASOUND SECTOR PROBES (PHASED ARRAY), MULTIDIMENSIONAL 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

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

Px 4-13 by Esaote S.p.A. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

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

Sources (1)

  • EUDAMED db33fcc3-895c-472e-b639-f5e549ef8d47 61 fields · synced Jun 18, 2026