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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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M04017 — 5 UDI-DI variants, MDR

MD Atlas
Intensiv Medical Products IMPROMEDIFORM GmbH

Data from EUDAMED, last updated May 23, 2026

M04017

4049051A03020101EAXXGXXCA

5 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: Intensiv Medical Products IMPROMEDIFORM GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4049051A03020101EAXXGXXCA
Device name: —
Device model: M04017
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: Intensiv Medical Products IMPROMEDIFORM GmbH
SRN: DE-MF-000014610
Country: Germany
Email: contact@imf.de
Phone: +49 2351 5506 500

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KS2SNYSG0NS08HC1W42X8T3B

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

M1711404049051074550
M1101104049051064100
M0407904049051012057
MF0000104049051000054
M0401704049051010503