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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

LR-15.2 W1 — Class I MDR by FAMED ŻYWIEC SP. Z O.O.

MD Atlas
FAMED ŻYWIEC SP. Z O.O.

EUDAMED last updated this device on Aug 12, 2024

LR-15.2 W1

59041572LR15MY

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: 05904157200014
Reference / catalog number: LR-15.2 W1

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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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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.

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

Device identification

Trade name: not provided
UDI-DI code: 05904157200014
Basic UDI-DI: 59041572LR15MY
Reference / catalog number: LR-15.2 W1
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

EMDN nomenclature code(s)

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

V08060101HOSPITAL/HOME CARE ELECTRIC MEDICAL BEDS

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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