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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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Mutliline next AC — 7 UDI-DI variants, MDR (Greiner GmbH)

MD Atlas
Greiner GmbH

Data from EUDAMED, last updated May 23, 2026

Mutliline next AC

40660984256Y

7 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: Greiner GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 40660984256Y
Device name: Mutliline next AC
Device model: 425
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 8, 2022

Manufacturer & authorised representative

Manufacturer

Name: Greiner GmbH
SRN: DE-MF-000007660
Country: Germany
Email: thomas.wegmann@greiner-gmbh.de
Phone: 07144/811241

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G9YZJV2ARCKEME2H0H87Y54W

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

425410504066098425077
425410904066098425015
425X00104066098425046
425410004066098425060
425411004066098425022
425X00304066098425053
425411504066098425039