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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

IV pole WK-17.2 — Class I MDR by FAMED ŻYWIEC SP. Z O.O.

MD Atlas
FAMED ŻYWIEC SP. Z O.O.

EUDAMED last updated this device on May 25, 2026

IV pole WK-17.2

59041572WK00NV

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: FAMED ŻYWIEC SP. Z O.O.
UDI-DI code: 05904157208539
Reference / catalog number: WK-17.2

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View device family (Basic UDI)

Manufacturer information

Organization name: FAMED ŻYWIEC SP. Z O.O.
SRN: PL-MF-000002794
Manufacturer status: Active

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WK-01.5 IV pole59041572AAIAKROn the market AS-08.0 Table top width extension59041572TTE24On the market AS-09.0 Leg holder59041572LSUZNOn the market AS-10.0 Arm support, angled59041572AR2On the market AS-11.0 Kneeling frame for proctology59041572PPCKOn the market

Certificates

Certificate health across this manufacturer's portfolio.

HZ 1436271-1Reissued
Quality management systemNotified body: 0197Expiry: Nov 13, 2030
HZ 1436271-1Issued
Quality management systemNotified body: 0197Expiry: Nov 13, 2025
TNP/MDR/003/0139/2022Issued
Quality management systemNotified body: 2274Expiry: Nov 13, 2025

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		Still on market

Device identification

Trade name: IV pole WK-17.2
UDI-DI code: 05904157208539
Basic UDI-DI: 59041572WK00NV
Reference / catalog number: WK-17.2
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: IV pole WK-17.2, chrome, angular, four metal hooks
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

EMDN nomenclature code(s)

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

V08068099MEDICAL BEDS - OTHER ACCESSORIES

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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