- Role
- Country
- Date of registration
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EUDAMED last updated this device on May 22, 2026
805969385KSTD-EMXMFCARRELLO EMERGENZA STANDARD IN ACCIAIO VERNICIATO CHIUSURA CON BARRA E SIGILLO, FIANCO DESTRO CON ALLOGGIO PORTA BOMBOLA is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by KARREL HEALTH SOLUTIONS SRL. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
IT-MF-000028683(01)08059693850265
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.
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 Italy; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | — | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
08059693850265Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
805969385KSTD-EMXMFKSTD-EM2UDI 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.
V0899MEDICAL SUPPORT EQUIPMENT - OTHERPrimary 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.
805969385K82026XXKJOn the marketCARRELLO EMERGENZA STANDARD CON STRUTTURA IN ACCIAIO INOX E 5 CASSETTI IN PLASTICA805969385K82026XXKJOn the marketCARRELLO EMERGENZA STANDARD CON STRUTTURA IN ACCIAIO VERNICI ATO E 5 CASSETTI IN PLASTICA805969385K82026XXKJOn the marketCARRELLO EMERGENZA STANDARD IN ACCIAIO VERNICIATO CON CHIUSU RA A SIGILLO E TAVOLA MASSAGGIO CARDIACO805969385KSTD-EMXMFOn the marketCARRELLO EMERGENZA STANDARD IN ACCIAIO VERNICIATO CON CHIUSURA A SIGILLO E TAVOLA MASSAGGIO CARDIACO, COMPLETO DI ALLOGGIO POSTERIORE PORTA BOMBOLA E MULTIPRESA ELETTRICA, FIANCO SINISTRO CON SUPPORTO PER POMPA ASPIRAZIONE E 2 TASCHE A RIBALTA805969385KSTD-EMXMFOn the marketCARRELLO EMERGIKAR IN ACCIAIO VERNICIATO CON CASSETTI ROSSI805969385K81622XDQOn the marketNo 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.