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US-MF-000002321G1 078838 0014 Rev.00External Paddles Water Resistant 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 4, 2026
B-20884838015245Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)20884838015245
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 | Mar 24, 2004 | Jan 19, 2023 |
| Belgium | Mar 24, 2004 | Jan 19, 2023 |
| Bulgaria | Mar 24, 2004 | Jan 19, 2023 |
| Cyprus | Mar 24, 2004 | Jan 19, 2023 |
| Czechia | Mar 24, 2004 | Jan 19, 2023 |
| Germany | Mar 24, 2004 | Jan 19, 2023 |
| Denmark | Mar 24, 2004 | Jan 19, 2023 |
| Estonia | Mar 24, 2004 | Jan 19, 2023 |
| EL | Mar 24, 2004 | Jan 19, 2023 |
| Spain | Mar 24, 2004 | Jan 19, 2023 |
| Finland | Mar 24, 2004 | Jan 19, 2023 |
| France | Mar 24, 2004 | Jan 19, 2023 |
| Croatia | Mar 24, 2004 | Jan 19, 2023 |
| Hungary | Mar 24, 2004 | Jan 19, 2023 |
| Ireland | Mar 24, 2004 | Jan 19, 2023 |
| Italy | Mar 24, 2004 | Jan 19, 2023 |
| Lithuania | Mar 24, 2004 | Jan 19, 2023 |
| Luxembourg | Mar 24, 2004 | Jan 19, 2023 |
| Latvia | Mar 24, 2004 | Jan 19, 2023 |
| Malta | Mar 24, 2004 | Jan 19, 2023 |
| Netherlands | Mar 24, 2004 | Jan 19, 2023 |
| Poland | Mar 24, 2004 | Jan 19, 2023 |
| Portugal | Mar 24, 2004 | Jan 19, 2023 |
| Romania | Mar 24, 2004 | Jan 19, 2023 |
| Sweden | Mar 24, 2004 | Jan 19, 2023 |
| Slovenia | Mar 24, 2004 | Jan 19, 2023 |
| Slovakia | Mar 24, 2004 | Jan 19, 2023 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
20884838015245Basic 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-20884838015245M3543AUDI 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.
Z12030580DEFIBRILLATORS - HARDWARE ACCESSORIESNo certificate specifically references this device's Basic UDI-DI.
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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.