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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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INm/IFm — 32 UDI-DI variants, MDR (Memmert GmbH + Co.KG)

MD Atlas
Memmert GmbH + Co.KG

Data from EUDAMED, last updated May 23, 2026

INm/IFm

42518175Im012GV

32 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: Memmert GmbH + Co.KG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 42518175Im012GV
Device name: INm/IFm
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: Memmert GmbH + Co.KG
SRN: DE-MF-000012127
Country: Germany
Email: info@memmert.com
Phone: +4991229250

Variants by status

UDI-DI variants

32 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KEECKZQ65CJGWP8KPEZE50DE

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

IF450m04251817500894
IF750m04251817500900
IF260mX204251817500962
IF110mX204251817500948
IN55mX204251817500764
IN30mX204251817500757
IF75m04251817500856

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