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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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Vingerspalk — 7 UDI-DI variants, MDR (Solutions company)

MD Atlas
Solutions company

Data from EUDAMED, last updated May 31, 2026

Vingerspalk

8721249549VSPLK0173

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: Solutions company

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8721249549VSPLK0173
Device name: Vingerspalk
Device model: VSPLK
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 1, 2026

Manufacturer & authorised representative

Manufacturer

Name: Solutions company
SRN: NL-MF-000051126
Country: Netherlands
Email: sc.contact.business@gmail.com
Phone: +31 6 11435300

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01KGC8P6WXDZ19PZWJKW3JGYBD

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

VSPLK-BGE 08721249549687
VSPLK-GRN 08721249549717
VSPLK-MBLW 08721249549908
VSPLK-RD 08721249549724
VSPLK-GL 08721249549700
VSPLK-ZWRT 08721249549731
VSPLK-BLW 08721249549694