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EUDAMED last updated this device on Feb 25, 2026
B-18719867001776Fluido® Compact Standard Set is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by The Surgical Company International B.V.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
18719867001776672000(01)18719867001776
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12030385INFUSION INSTRUMENTS - CONSUMABLES1 warning recorded — scroll inside the panel to see all entries.
NL-MF-0000019732081762CE03Primary placement in Netherlands; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | — | Still on market |
| Germany | — | Still on market |
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.
8719867EMDNZ12030380AGHXOn the marketFluido® Compact Control ModuleB-18719867001554On the marketFluido® Compact Holder for Warming Module8719867EMDNV0899FCHJMOn the marketFluido® Compact Warming ModuleB-18719867001561On the marketFluido® Compressor8719867EMDNZ12030380CQWOn the marketFluido® Irrigation Catheter ConnectorB-18719867001936On the marketCertificate health across this manufacturer's portfolio.
2259019CE01Supplemented2259019CE02Amended2259019CE03AmendedNotified 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 →Notified 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 →Notified 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 →