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US-MF-000002321MX40 Adapter 5L+SpO2 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. 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 May 26, 2026
0884838BM332SNPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)00884838082205
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
2 warnings recorded — scroll inside the panel to see all entries.
Consult IFU
These cables are not suitable for use in an MRI environment which could create a potential for patient burns or inaccurate measurements.
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 27 countries total.
| Country | On market since | Until |
|---|---|---|
| AustriaPrimary placement | Apr 17, 2017 | Dec 18, 2027 |
| Belgium | Apr 17, 2017 | Dec 18, 2027 |
| Bulgaria | Apr 17, 2017 | Dec 18, 2027 |
| Cyprus | Apr 17, 2017 | Dec 18, 2027 |
| Czechia | Apr 17, 2017 | Dec 18, 2027 |
| Germany | Oct 11, 2016 | Dec 18, 2027 |
| Denmark | Apr 17, 2017 | Dec 18, 2027 |
| Estonia | Apr 17, 2017 | Dec 18, 2027 |
| EL | May 26, 2020 | Dec 18, 2027 |
| Spain | Apr 17, 2017 | Dec 18, 2027 |
| Finland | Apr 17, 2017 | Dec 18, 2027 |
| France | Apr 17, 2017 | Dec 18, 2027 |
| Croatia | Apr 17, 2017 | Dec 18, 2027 |
| Hungary | Apr 17, 2017 | Dec 18, 2027 |
| Ireland | Apr 17, 2017 | Dec 18, 2027 |
| Italy | Apr 17, 2017 | Dec 18, 2027 |
| Lithuania | Apr 17, 2017 | Dec 18, 2027 |
| Luxembourg | Apr 17, 2017 | Dec 18, 2027 |
| Latvia | Apr 17, 2017 | Dec 18, 2027 |
| Malta | Apr 17, 2017 | Dec 18, 2027 |
| Netherlands | Apr 17, 2017 | Dec 18, 2027 |
| Poland | Apr 17, 2017 | Dec 18, 2027 |
| Portugal | Apr 17, 2017 | Dec 18, 2027 |
| Romania | Apr 17, 2017 | Dec 18, 2027 |
| Sweden | Oct 11, 2016 | Dec 18, 2027 |
| Slovenia | Apr 17, 2017 | Dec 18, 2027 |
| Slovakia | Apr 17, 2017 | Dec 18, 2027 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
00884838082205Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
0884838BM332SN989803199091UDI 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.
Z1203020202TRANSPORTABLE/PORTABLE MULTI–PARAMETER PATIENT MONITORSB-00884838030350On the marketMX40 Adapter 3L+SpO20884838BM332SNOn the marketMX40 Adapter 5-Lead + Masimo SpO20884838BM332SNOn the marketMX40 Adapter 6-Lead + Masimo SpO20884838BM332SNOn the marketMX40 Adapter 6L+SpO20884838BM332SNOn the marketMX40 Adapter Masimo SpO2-only0884838BM332SNOn the marketNo certificate specifically references this device's Basic UDI-DI.
No 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.