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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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Uchwyt ręki UR-07 / Hand grip UR-07 — 3 UDI-DI variants, MDR

MD Atlas
FAMED ŻYWIEC SP. Z O.O.

Data from EUDAMED, last updated May 30, 2026

Uchwyt ręki UR-07 / Hand grip UR-07

59041572UR0700FK

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: FAMED ŻYWIEC SP. Z O.O.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 59041572UR0700FK
Device name: Uchwyt ręki UR-07 / Hand grip UR-07
Device model: UR-07
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: FAMED ŻYWIEC SP. Z O.O.
SRN: PL-MF-000002794
Country: Poland
Email: sekretariat@famed.com.pl
Phone: +48 33 866 62 00

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KS7C58VYRS41MPTQSFY9V2T0

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

UR-07.0 Hand grip chrome05904157208560
UR-07.2 Hand grip powder coated05904157208577
UR-07.4 Hand grip rollable05904157208584