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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 — 7 UDI-DI variants, MDR

MD Atlas
Allion BV h.o.d.n. van Heek Medical

Data from EUDAMED, last updated May 30, 2026

Non-woven swab

8715886NonWovenKompresKM

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: Allion BV h.o.d.n. van Heek Medical

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8715886NonWovenKompresKM
Device name: Non-woven swab
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 8, 2024

Manufacturer & authorised representative

Manufacturer

Name: Allion BV h.o.d.n. van Heek Medical
SRN: NL-MF-000003490
Country: Netherlands
Email: info@vanheekmedical.nl
Phone: +31 88 220 88 22

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HP4FJC5KMNA2605AZ14XTJJ9

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

NK058008715886008386
NK025008715886000434
NK028008715886006382
NK037008715886001127
NK054008715886006047
NK072008715886000472
NK051008715886000458