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EUDAMED last updated this device on Apr 7, 2023
5944759042000179IDSXIRIGATOR DEEA is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by SC MEDDO SRL. Placed on the EU market in Romania. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
059447590420328920(01)05944759042032
European Medical Device Nomenclature — the EU product classification assigned to this device.
A03040299IRRIGATION KITS, SINGLE-USE - OTHERPrimary placement in Romania; available across 1 country total.
Placed on the market in Romania; per-country availability dates not published.
RO-MF-000018753The 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 →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
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 →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.
View in glossary →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.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.
594475904264252950001009EOn the marketCOPRORECOLTOR CU SPATULA PS594475904264252950001249UOn the marketIRIGATOR5944759042000032IRRHOn the marketMINIIRIGATOR5944759042000049MINZ9On the marketPOMPA LAPTE5944759042000025POLYLOn the marketRECOLTOR URINA DE 60 ML59447590426425295000155A7On the market