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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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Slip voet — 3 UDI-DI variants, MDR (Independent Special Products BV)

MD Atlas
Independent Special Products BV

Data from EUDAMED, last updated May 30, 2026

Slip voet

871932695583010X6

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: Independent Special Products BV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 871932695583010X6
Device name: Slip voet
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 1, 2024

Manufacturer & authorised representative

Manufacturer

Name: Independent Special Products BV
SRN: NL-MF-000006047
Country: Netherlands
Email: sales@eritekbv.nl
Phone: +31859020266

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JB1FW5HHH6PQNGHJXCSTENYH

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

301008719326955865
301108721082370172
300308721082370752