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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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Organization name
UDI-DI code
Reference / catalog number

NF-KNIEBANDAGE-ZWART — Class I MDR by SPRONKEN ORTHOPEDIE

MD Atlas
SPRONKEN ORTHOPEDIE

EUDAMED last updated this device on Feb 16, 2026

NF-KNIEBANDAGE-ZWART

1169154KNE04PW

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SPRONKEN ORTHOPEDIE
UDI-DI code: 08720589780132
Reference / catalog number: NF-KNIEBANDAGE-ZWART

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Manufacturer information

Organization name: SPRONKEN ORTHOPEDIE
SRN: BE-MF-000003430
Manufacturer status: Active

Related devices

QS-UOMO-S/M1169154UOM07UZOn the market NF-KNIEBANDAGE-COLD21169154KNE04PWOn the market NF-KNIEBANDAGE-KLEIN1169154KNE04PWOn the market NF-KAAKBANDAGE-COLD1169154JAW06PNOn the market NF-SHOULDERBAND-COLD1169154SHO05SYOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Market distribution

Primary placement in Belgium; available across 1 country total.

Placed on the market in Belgium; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 08720589780132
Basic UDI-DI: 1169154KNE04PW
Reference / catalog number: NF-KNIEBANDAGE-ZWART
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y061209KNEE ORTHOSES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
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Software identification