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EUDAMED last updated this device on May 25, 2026
84356058UDI-DI-156B120ML PP CUPPED CONTAINER 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.
08435263876789409702.PES-MF-000000153(01)08435263876789
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.
• 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. Healthcare professionals must validate the use of the container for their specific assay-instrument/reagent system combinations and specimen storage conditions.
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 2 countries total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | — | Still on market |
| France | — | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
W05019099SAMPLES COLLECTION DEVICES - 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 →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 →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.
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 →84356058UDI-DI-156BOn the market120ML CONTAINER PP WITH SPOON84356058UDI-DI-156BOn the market120ML PP CONTAINER LABELLED84356058UDI-DI-156BOn the market120ML PP CUPPED CONTAINER WHITE C.84356058UDI-DI-156BOn the market15ML CONICAL TUBE PP84356058UDI-DI-156BOn the market15ml CONICAL TUBE PP SEP.CAP84356058UDI-DI-156BOn the marketNo 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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