- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Nov 27, 2023
8719689142QMAPPCONSKJQMAPP AUX cable to bipolar touch-protected 2mm inline socket 3 M is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Fysicon B.V.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0872025454270601076503NL-MF-000002694(01)08720254542706
The 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.
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 Netherlands; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | — | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12050785INSTRUMENTS FOR CARDIOLOGICAL POLYGRAPHY - CONSUMABLESPrimary 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 →8719689142QMAPPCONSKJOn the marketQMAPP 5 Lead ECG Trunk cable, IEC 320 CM8719689142QMAPPCONSKJOn the marketQMAPP AUX cable to 6.3 mm Mono Jack for Volcano i5, Black 165 CM8719689142QMAPPCONSKJOn the marketQMAPP AUX to BNC cable8719689142QMAPPCONSKJOn the marketQMAPP Cardiac Output In-line Injectate Temperature probe8719689142QMAPPCONSKJOn the marketQMAPP Cardiac Output Y-connection cable8719689142QMAPPCONSKJOn the marketNo certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
24M00192CRT01Reissued24M00192CRT01Reissued21M00066CRT02AmendedNotified 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 →