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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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P2 5-13 — 1 UDI-DI variant, MDD (Esaote S.p.A.)

MD Atlas
Esaote S.p.A.

Data from EUDAMED, last updated May 30, 2026

P2 5-13

B-08056304453082

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: Esaote S.p.A.

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Device characteristics

Active device

Legacy certificates

Certificate number: G1 095545 0023
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: TÜV SÜD Product Service GmbH (0123)
Validity: May 25, 2024

Identity & classification

Basic UDI-DI: B-08056304453082
Device name: P2 5-13
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Nov 11, 2022

Manufacturer & authorised representative

Manufacturer

Name: Esaote S.p.A.
SRN: IT-MF-000019024
Country: Italy
Email: qa@esaote.com
Phone: +3901065471

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01FXA0P12RJAPHYQ9MKT3EZE9D

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

12000004408056304453082