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Organization name
UDI-DI code
Reference / catalog number

URGO BANDE DE KINESIOLOGIE — Class I MDR by Fink & Walter GmbH

MD Atlas
Fink & Walter GmbH

EUDAMED last updated this device on May 6, 2026

URGO BANDE DE KINESIOLOGIE

4260348612361VC

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Fink & Walter GmbH
UDI-DI code: 04262495682024
Reference / catalog number: 552698

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Manufacturer information

Organization name: Fink & Walter GmbH
SRN: DE-MF-000000692
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
Leaflet with instrucion for use is included in the box

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement	Oct 10, 2018	Still on market
France	Oct 10, 2018	Still on market

Device identification

Trade name: URGO BANDE DE KINESIOLOGIE
UDI-DI code: 04262495682024
Basic UDI-DI: 4260348612361VC
Reference / catalog number: 552698
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: Elastic TAPE for kinesiological therapy "URGO BANDE DE KINESIOLOGIE" 5cm x 5m, single box with window including leaflet
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 5 MU10
5 MU36

EMDN nomenclature code(s)

M030403FUNCTIONAL BANDAGES WITH ANELASTIC TAPES

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
Manufacturing date
Serial number
Software identification

Related devices

URGO BANDE DE KINESIOLOGIE4260348612361VCOn 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.