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ES-MF-000000153SECURITY CONTAINER 90ML(Ø53-h68) is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Deltalab, S.L.. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on May 16, 2026
84356058UDI-DI-156BPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)08435263806793
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
2 warnings recorded — scroll inside the panel to see all entries.
Healthcare professionals must validate the use of the container for their specific assay-instrument/reagent system combinations and specimen storage conditions.
• Not suitable for any application other than its intended use. • Do not squeeze or press the container. • Do not use if the product or any of its components is damaged. • Do not re-use. The re-use of this product may affect the subsequent analysis of the sample taken.
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.
Primary placement in Spain; available across 16 countries total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | Feb 23, 2007 | Still on market |
| Belgium | Feb 11, 2020 | Still on market |
| Bulgaria | Sep 23, 2014 | Still on market |
| Czechia | Jul 5, 2013 | Still on market |
| Germany | Jan 30, 2013 | Still on market |
| Denmark | Jan 24, 2013 | Still on market |
| Estonia | Jul 11, 2013 | Still on market |
| EL | Feb 28, 2020 | Still on market |
| Finland | May 30, 2018 | Still on market |
| France | Jan 30, 2013 | Still on market |
| Croatia | Apr 25, 2014 | Still on market |
| Italy | Jan 31, 2014 | Still on market |
| Portugal | Feb 1, 2013 | Still on market |
| Romania | Jan 20, 2015 | Still on market |
| Slovenia | Aug 5, 2013 | Still on market |
| Slovakia | May 23, 2013 | 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.
08435263806793Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
84356058UDI-DI-156B202848UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
IVDR risk classes
IVDR risk classes rank in-vitro diagnostic devices from lowest risk (Class A) to highest (Class D), based on the patient and public-health risk of a wrong result.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W05019099SAMPLES COLLECTION DEVICES - OTHERNo certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
2024 PR 0038IssuedNotified 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.
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