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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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Non-woven swab — 3 UDI-DI variants, MDR (Fleming Medical )

MD Atlas
Fleming Medical

Data from EUDAMED, last updated May 24, 2026

Non-woven swab

5099390SwabHL

3 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: Fleming Medical

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5099390SwabHL
Device name: Non-woven swab
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 3, 2025

Manufacturer & authorised representative

Manufacturer

Name: Fleming Medical
SRN: IE-MF-000044303
Country: Ireland
Email: quality@flemingmedical.ie
Phone: +35361304600

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01JNDDX6N17B95JWKQ9DBBPJ8Y

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

Mediswab Non-Sterile Non-Woven Swabs05099390403404
Mediswab Non-Sterile Non-Woven Swabs05099390403411
Mediswab Non-Sterile Non-Woven Swabs05099390403398