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EUDAMED last updated this device on Aug 10, 2022
843702490901EGAilin Kit is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Home Diagnostics S.L. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0843702490901901(01)08437024909019
European Medical Device Nomenclature — the EU product classification assigned to this device.
A99DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - OTHER7 warnings recorded — scroll inside the panel to see all entries.
if pregnant, of coagulation issue or if you are taking anticoagulant medication ask your doctor before using this kit
The reactive in one of the microtubes is from animal origin
One use only
book information symbol in the packaging A
Crossed box symbol in instructions
date indicated in packaging
Primary placement in Spain; available across 1 country total.
Placed on the market in Spain; per-country availability dates not published.
ES-MF-000026858The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
if you tend to feel dizzy when seeing blood. Check with your doctor before using the device and do not do it on your own
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.