- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Mar 20, 2026
42510422HMP6100ZUMIB is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Hegewald Medizinprodukte GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0425104221306410215453 packaging levels registered — each level carries its own UDI-DI.
04251042213064× 1 unitBase unit04251042213071× 1 unit04251042213088× 20 units04251042213095× 2 units(01)04251042213064
European Medical Device Nomenclature — the EU product classification assigned to this device.
A080102PARENTERAL FEEDING BAGS AND CONTAINERS (INCLUDING THOSE VIA PUMP), SINGLE-USE5 warnings recorded — scroll inside the panel to see all entries.
Gebrauchsanweisung beachten
Mehrfache Verwendung hat negative Auswirkungen auf die Funktion des Produktes und kann zur Patientengefährdung führen.
Mehrfache Sterilisation von gebrauchten Beuteln ist nicht zulässig.
Die Beutel sind nicht zu verwenden, wenn die Verpackung beschädigt ist, die Schutzkappen an den Anschlüssen fehlen oder andere Auffälligkeiten die Unbrauchbarkeit des Produktes vermuten lassen.
Nach Ablauf des Haltbarkeitsdatums ist das Produkt zu entsorgen und nicht mehr zu verwenden.
Primary placement in Germany; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | — | Still on market |
DE-MF-000006219The 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 certificate specifically references this device's Basic UDI-DI.
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 →Certificate health across this manufacturer's portfolio.
2608GB448230509IssuedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →