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HU-MF-000006381Sterilizing container with red lid, perforated on top, 580x280x200 mm is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by SUBAN Kéziműszer Hungary Zártkörűen Működő Részvénytársaság. Placed on the EU market in Hungary. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on May 26, 2026
5996660Steriliz_egysegE5Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)05996660060599
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 Hungary; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| HungaryPrimary 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.
05996660060599Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
5996660Steriliz_egysegE5RT-502-20UDI 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.
S010499STERILISATION CONTAINERS - OTHERCertificate health across this manufacturer's portfolio.
25 0316 QA/NBIssuedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
5996660Steriliz_egysegE5On the marketSterilizing container with red lid, perforated on top, 580x280x135 mm5996660Steriliz_egysegE5On the marketSterilizing container with red lid, perforated on top, 580x280x150 mm5996660Steriliz_egysegE5On the marketSterilizing container with red lid, perforated on top, 580x280x260 mm5996660Steriliz_egysegE5On the marketSterilizing container with red lid, perforated top and bottom, 285x280x100 mm5996660Steriliz_egysegE5On the marketSterilizing container with red lid, perforated top and bottom, 285x280x135 mm5996660Steriliz_egysegE5On the market