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US-MF-000002321G1 044649 0046MX40 - 2.4 is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Philips Medical Systems. Placed on the EU market in Austria. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Jun 11, 2025
B-00884838082243Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)00884838082243
1 warning recorded — scroll inside the panel to see all entries.
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 Austria; available across 24 countries total.
| Country | On market since | Until |
|---|---|---|
| AustriaPrimary placement | May 17, 2019 | Still on market |
| Belgium | May 17, 2019 | Still on market |
| Bulgaria | May 17, 2019 | Still on market |
| Cyprus | May 17, 2019 | Still on market |
| Czechia | May 17, 2019 | Still on market |
| Germany | May 17, 2019 | Still on market |
| Denmark | May 17, 2019 | Still on market |
| Estonia | May 17, 2019 | Still on market |
| EL | May 17, 2019 | Still on market |
| Spain | May 17, 2019 | Still on market |
| Finland | May 17, 2019 | Still on market |
| France | May 17, 2019 | Still on market |
| Hungary | May 17, 2019 | Still on market |
| Ireland | May 17, 2019 | Still on market |
| Italy | May 17, 2019 | Still on market |
| Lithuania | May 17, 2019 | Still on market |
| Luxembourg | May 17, 2019 | Still on market |
| Latvia | May 17, 2019 | Still on market |
| Malta | May 17, 2019 | Still on market |
| Netherlands | May 17, 2019 | Still on market |
| Poland | May 17, 2019 | Still on market |
| Portugal | May 17, 2019 | Still on market |
| Romania | May 17, 2019 | Still on market |
| Sweden | May 17, 2019 | 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.
00884838082243Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
B-00884838082243865351UDI 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.
Z12050803ELECTROCARDIOGRAPH TELEMETRY SYSTEM TRANSMITTERS0884838BM511SQOn the marketLrg Switched Int PdlsB-00884838094734On the marketMedium Switched Int PdlsB-00884838094741On the marketMX40 - WLANB-00884838030350On the marketMX40 Adapter 3L+SpO20884838BM332SNOn the marketMX40 Adapter 5-Lead + Masimo SpO20884838BM332SNOn the marketNo certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.No certificate specifically references this device's Basic UDI-DI.