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EUDAMED last updated this device on Jul 13, 2026
803377232CAT-U0502MJ2-ways LONG CARLIER catheter in PEBAX, 8Fr is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Medica S.p.A.. Placed on the EU market in Austria. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
080569923337342CYS-8ESF2 packaging levels registered — each level carries its own UDI-DI.
08056992333734× 1 unitBase unit18056992333731× 10 units28056992333738× 30 unitsIT-MF-000025691(01)08056992333734
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
6 warnings recorded — scroll inside the panel to see all entries.
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.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Austria; available across 8 countries total.
| Country | On market since | Until |
|---|---|---|
| AustriaPrimary placement | Jun 1, 2023 | Still on market |
| Germany | Jun 1, 2023 | Still on market |
| Spain | Jun 1, 2023 | Still on market |
| France | Jun 1, 2023 | Still on market |
| Ireland | Jun 1, 2023 | Still on market |
| Italy | Jun 1, 2023 | Still on market |
| Netherlands | Jun 1, 2023 | Still on market |
| Portugal | Jun 1, 2023 | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
U050201FILLING CATHETERS FOR URINARY PRESSURE-FLOW STUDYPrimary 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 →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.
803377232CAT-U0504MNOn the market2-way catheter for cystometry - PFS in PVC, soft, 8 Fr with Blue line803377232CAT-U0502MJOn the market2-way catheter for cystometry - PFS in PVC, soft, 8 Fr with Blue line803377232CAT-U0502MJOn the market21 with 4 Hansen (2 open - 2 closed) - EO803377232ULT-DIANBOn the market28 with 4 Hansen (3 open - 1 closed) - EO803377232ULT-DIANBOn the market2AR-12MX Catheter803377232CAT-U0504MNOn the marketNo 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.