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EUDAMED last updated this device on Jun 11, 2026
735015095M4PFZMulti4 Pump is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Multi4 Medical AB. Placed on the EU market in Sweden. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
07350150950025M4P00(01)07350150950025
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12010999ELECTROSURGERY INSTRUMENTS - OTHER1 warning recorded — scroll inside the panel to see all entries.
Observe the bladder while using the FILL function to avoid over- extending the bladder. The FILL function is not pressure controlled. Use the accessories provided with and specified for the Multi4 System. Using other accessories can pose a safety risk. To avoid the risk of electric shock the equipment must only be connected to a supply mains with protective earth. Do not use Multi4 system outside the recommended ESU output specified. Material might degrade by use outside limits and safety and performance are not verified with output outside of recommended range. Do not modify the Multi4 Pump or remove the enclosure. Do not use Portable RF communications equipment (including peripherals such as antenna cables and external cables) closer than 30 cm (12 inches) to any part of the Multi4 system. Otherwise, the performance cannot be guaranteed. Multi4 System should not be used in the presence of flammable liquids, in an oxygen enriched atmosphere or in the presence of explosive gases. The patient should not be allowed to come into direct contact with grounded metal objects (e.g. surgical table frames, instrument tables etc. This can cause alternate site burns.
Primary placement in Sweden; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| SwedenPrimary placement | Aug 10, 2026 | Still on market |
SE-MF-000051746The 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 →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.
Certificate health across this manufacturer's portfolio.
28620244520SupplementedNotified 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 →