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EUDAMED last updated this device on Feb 3, 2026
570859035585R11WDVALUE II toiletstøtte, 850 mm, fast højde, montering til højre for bruger, inkl. betjeningspanel til elektrisk toiletløfter, hvid is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Pressalit A/S. Placed on the EU market in Denmark. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
DK-MF-000001767(01)57085903564888
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Denmark; available across 1 country total.
Placed on the market in Denmark; per-country availability dates not published.
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
57085903564888Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
570859035585R11WDR1104000UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Y181809ARMRESTSPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →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.No certificate specifically references this device's Basic UDI-DI.
570859035585R11WDOn the marketVALUE II support arm, 850 mm, white. Fixed height, wall-mounted570859035585R11WDOn the marketVALUE II support arm, 850 mm, white. Height adjustable, wall-mounted570859035585R11WDOn the marketVALUE II toiletstøtte, 850 mm, fast højde, montering til venstre for bruger, hvid570859035585R11WDOn the marketVALUE IV backrest, 353 mm, anthracite. Fixed height, wall-mounted570859031062R16R7On the marketVALUE IV folding shower seat, 440 mm, anthracite. Fixed height, wall-mounted570859034936R16WAOn the market