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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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IES 3 smoke evacuation unit — 3 UDI-DI variants, MDR

MD Atlas
Erbe Elektromedizin GmbH

Data from EUDAMED, last updated May 23, 2026

IES 3 smoke evacuation unit

4050147IES3-K4

3 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: Erbe Elektromedizin GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4050147IES3-K4
Device name: IES 3 smoke evacuation unit
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: Erbe Elektromedizin GmbH
SRN: DE-MF-000005498
Country: Germany
Email: Ralf.Mack@erbe-med.com
Phone: 004916093969516

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRGA5S4KD4WW2D7R52S4MGK8

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

Evacuation funnel connection04050147007482
Evacuation tube, optimized for04050147007437
IES 304050147022140