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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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KNEE BANDAGE — 3 UDI-DI variants, MDR (SPRONKEN ORTHOPEDIE)

MD Atlas
SPRONKEN ORTHOPEDIE

Data from EUDAMED, last updated May 23, 2026

KNEE BANDAGE

1169154KNE04PW

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: SPRONKEN ORTHOPEDIE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 1169154KNE04PW
Device name: KNEE BANDAGE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 16, 2026

Manufacturer & authorised representative

Manufacturer

Name: SPRONKEN ORTHOPEDIE
SRN: BE-MF-000003430
Country: Belgium
Email: frank.iliaens@spronken.com
Phone: +3289500500

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KHK9NZ9YKKAA1ZAQWG42W9JB

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

NF-KNIEBANDAGE-KLEIN08720589780118
NF-KNIEBANDAGE-COLD208720589780125
NF-KNIEBANDAGE-ZWART08720589780132