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EUDAMED last updated this device on Jul 2, 2026
803377232INF-HTPEJLinea per perfusione ipertermica / Hyperthermal perfusion line 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 Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
IT-MF-000025691(01)08033772322478
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 Italy; available across 8 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Jun 1, 2023 | Still on market |
| Austria | 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 |
| Netherlands | Jun 1, 2023 | Still on market |
| Portugal | Jun 1, 2023 | Still on market |
| XI | Jun 1, 2023 | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
08033772322478Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
803377232INF-HTPEJM03230UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
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.
1 packaging level registered — each level carries its own UDI-DI.
08033772322478× 1 unitBase unit28033772322472× 6 unitsEuropean Medical Device Nomenclature — the EU product classification assigned to this device.
A030499ADMINISTRATION KITS - 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 →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.803377232ADSH2On the marketLinea HDF senza filtro / HDF Line without filter803377232INF-DRL-ETO-YTOn the marketLinea mandata / Delivery line803377232INF-HTPEJOn the marketLinea per trattamento di ECCO2R + HF803377232HMF-SETE6On the marketLinea pompa aspirazione per Flexiper / Aspiration pump line for Flexiper803377232INF-HTPEJOn the marketLINEA UNICA AD ALTO FLUSSO PERFUSIONE VENA FEGATO803377232INF-ORPFFOn the marketNo certificate specifically references this device's Basic UDI-DI.