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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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Evo IQ Syringe Infusion Pump — 4 UDI-DI variants, MDR

MD Atlas
Baxter Healthcare SA

Data from EUDAMED, last updated May 23, 2026

Evo IQ Syringe Infusion Pump

0085412GMN000000000021372

4 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Baxter Healthcare SA

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Device characteristics

Active deviceAdministers medicine

Identity & classification

Basic UDI-DI: 0085412GMN000000000021372
Device name: Evo IQ Syringe Infusion Pump
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: Nov 21, 2025

Manufacturer & authorised representative

Manufacturer

Name: Baxter Healthcare SA
SRN: CH-MF-000026124
Country: Switzerland
Email: simone_diorio@baxter.com
Phone: +41 (79) 4413671

Authorised representative

Name: Baxter Deutschland GmbH
SRN: DE-AR-000010308
Country: Germany
Phone: +49 89 317010

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KAM3BPCASE5QRHZ2R2XKQSZJ

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

EVO IQ05413765939259
EVO IQ05413765939327
EVO IQ05413765581816
EVO IQ05413765581809