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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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ACLMI001memf — 4 UDI-DI variants, MDR (seca gmbh & co. kg)

MD Atlas
seca gmbh & co. kg

Data from EUDAMED, last updated May 23, 2026

ACLMI001memf

401203000000000000036QS

4 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: seca gmbh & co. kg

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Device characteristics

Measuring function

Identity & classification

Basic UDI-DI: 401203000000000000036QS
Device name: —
Device model: ACLMI001memf
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 16, 2026

Manufacturer & authorised representative

Manufacturer

Name: seca gmbh & co. kg
SRN: DE-MF-000005469
Country: Germany
Email: info@seca.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KPAWPXJEKNQ07EJ3X7R9PZH8

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

220171400304012030018647
220181400304012030018685
223181499804012030018753
223171799804012030018746