- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on May 24, 2022
5744003280STRIP6MStripping buffer, 100 mL is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by RefLab Aps. Placed on the EU market in Denmark. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
05744003280261RLA701(01)05744003280261
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0201020285LIMITED PANEL IMMUNOCHEMISTRY ANALYSERS - CONSUMABLES1 warning recorded — scroll inside the panel to see all entries.
See Instructions for Use and Safety Data Sheet
Primary placement in Denmark; available across 1 country total.
Placed on the market in Denmark; per-country availability dates not published.
DK-MF-000021844The 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.
View in glossary →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.
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 →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 →No certificate specifically references this device's Basic UDI-DI.
No 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.574400328STOPFWOn the marketStop reagent (HClO4), 100 mL574400328STOPFWOn the marketStripping buffer 1 L5744003280STRIP6MOn the marketWash buffer 200 mL574400328WASHDPOn the marketWash buffer 5 L574400328WASHDPOn the marketWash buffer concentrate 10 mL574400328WASHDPOn the market