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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

DF WW-001 — Class I MDR by Medical Sport…

MD Atlas
Medical Sport Bartłomiej Flis

EUDAMED last updated this device on Apr 30, 2026

DF WW-001

590393808silo3W

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Medical Sport Bartłomiej Flis
UDI-DI code: 05903938081699
Reference / catalog number: DF WW-001

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View device family (Basic UDI)

Manufacturer information

Organization name: Medical Sport Bartłomiej Flis
SRN: PL-MF-000005380
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Poland; available across 1 country total.

Country	On market since	Until
PolandPrimary placement	Jul 3, 2023	Still on market

Device identification

Trade name: not provided
UDI-DI code: 05903938081699
Basic UDI-DI: 590393808silo3W
Reference / catalog number: DF WW-001
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.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05903938081699

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Y060609WRIST (FOREARM) 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

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Related devices

MS910-41590393808wm5MOn the market MS910-51590393808wm5MOn the market DF 1161, DF 1162, DF 1163, DF 1164590393808115xAUOn the market DF 1171, DF 1172, DF 1173, DF 1174590393808115xAUOn the market DF 1151, DF 1152, DF 1153, DF 1154590393808115xAUOn 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.