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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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Gauze Swabs, invasive, sterile — 13 UDI-DI variants, MDR

MD Atlas
Lohmann & Rauscher International GmbH & Co. KG

Data from EUDAMED, last updated May 31, 2026

Gauze Swabs, invasive, sterile

4021447-0001-JM

13 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: Lohmann & Rauscher International GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4021447-0001-JM
Device name: —
Device model: Gauze Swabs, invasive, sterile
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Lohmann & Rauscher International GmbH & Co. KG
SRN: DE-MF-000005052
Country: Germany
Email: info@de.lrmed.com

Variants by status

UDI-DI variants

13 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS7W3N14WFJKQ438A1HH6697

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

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1667704021447353012
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3592104068225060014
3591804068225059988
3586504068225059957
3581204068225059834
3580904068225059803
3599104068225060045
3586304068225059926
3599504068225060076
3585004068225059896
3581504068225059865