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EUDAMED last updated this device on Mar 6, 2026
084399700000Z7T0C01V007LPLiDCO to MR MPM, Analog Cable is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Masimo Corporation. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
US-MF-000010641(01)00843997002653
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 Germany; available across 9 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | — | Still on market |
| Belgium | — | Still on market |
| Spain | — | Still on market |
| France | — | Still on market |
| Italy | — | Still on market |
| Netherlands | — | Still on market |
| Norway | — | Still on market |
| Poland | — | Still on market |
| Türkiye | — | 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.
00843997002653Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
084399700000Z7T0C01V007LP5134UDI 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.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12050702POLYGRAPHY SYSTEMS FOR HAEMODYNAMIC STUDIESPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →084399700000Z7T0C01V006LMOn the marketLiDCO to MR Benevision, Analog Cable084399700000Z7T0C01V007LPOn the marketLiDCO to MR iPM, Analog Cable084399700000Z7T0C01V007LPOn the marketLiDCO to MR T5 to T9, Analog Cable084399700000Z7T0C01V007LPOn the marketLiDCO to NK, Analog Cable084399700000Z7T0C01V007LPOn the marketLiDCO to Philips, Analog Cable084399700000Z7T0C01V007LPOn the marketCertificate health across this manufacturer's portfolio.
28620149254-03SupplementedNotified 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 →No certificate specifically references this device's Basic UDI-DI.