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- Date of registration
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EUDAMED last updated this device on Jun 12, 2026
805771123SEDIEPORTANT5HMOD.P024 SPENCER 458 SEDIA PORTANTINA TELO NERO is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Spencer Italia s.r.l.. Placed on the EU market in Hungary. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08057711231935ST36462IT-MF-000027507No 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.(01)08057711231935
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
1 warning recorded — scroll inside the panel to see all entries.
CW010Sterile
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 Hungary; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| HungaryPrimary placement | — | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
V080202MANUAL MEDICAL CHAIRSPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →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.
View in glossary →Primary 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 certificate specifically references this device's Basic UDI-DI.
805771123SEDIEPORTANT5HOn the marketMOD.O004 UNICA TORION SEDIA PORTANTINA C/BRACC805771123SEDIEPORTANT5HOn the marketMOD.P024 SPENCER 458 SEDIA PORTANTINA TELO GIALLO805771123SEDIEPORTANT5HOn the marketMOD.P028 BARELLINO805771123BARELLEDACAMPOGROn the marketMOD.R015 SKID-E SEDIA EVACUAZIONE NERA805771123SEDIEVACUAZX8On the marketMOD.S003 SPENCER TWIN SHELL ARANCIO BARELLA805771123BASKETACRWOn the market