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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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EPSA Series — 6 UDI-DI variants, MDR (IGEA S.p.A.)

MD Atlas
IGEA S.p.A.

Data from EUDAMED, last updated May 31, 2026

EPSA Series

805004099EPSA8Q

6 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: IGEA S.p.A.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805004099EPSA8Q
Device name: EPSA Series
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: IGEA S.p.A.
SRN: IT-MF-000011242
Country: Italy
Email: c.guerrieri@igeamedical.com
Phone: +39059699600

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KG24SMWAAEPRSHWQC402HV28

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

EPSA Series58050040991070
IGE06058050040991094
EPSA Series58050040991100
EPSA Series58050040991124
EPSA Series58050040991087
EPSA Series58050040991117