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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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P04 — 2 UDI-DI variants, MDR (DUNA s.r.l.)

MD Atlas
DUNA s.r.l.

Data from EUDAMED, last updated May 31, 2026

P04

805071407P04D3

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: DUNA s.r.l.

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Device characteristics

Animal tissues / cells

Identity & classification

Basic UDI-DI: 805071407P04D3
Device name: —
Device model: P04
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: DUNA s.r.l.
SRN: IT-MF-000010174
Country: Italy
Email: info@duna.it
Phone: +39 71 918073

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KPQPR481JFFCMP03X3SFR7NB

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

WM19 ELETTA08058425561127
WM19 ELETTA08058425561134