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US-MF-000002301DreamStation Shielded DC Cord System is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Respironics Inc.. Placed on the EU market in Belgium. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Jan 25, 2025
0606959BM224LUPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)00606959412958
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 Belgium; available across 27 countries total.
| Country | On market since | Until |
|---|---|---|
| BelgiumPrimary placement | May 23, 2018 | Dec 31, 9999 |
| Austria | May 23, 2018 | Dec 31, 9999 |
| Cyprus | May 23, 2018 | Dec 31, 9999 |
| Czechia | May 23, 2018 | Dec 31, 9999 |
| Germany | May 23, 2018 | Dec 31, 9999 |
| Denmark | May 23, 2018 | Dec 31, 9999 |
| Estonia | May 23, 2018 | Dec 31, 9999 |
| EL | May 23, 2018 | Dec 31, 9999 |
| Spain | May 23, 2018 | Dec 31, 9999 |
| Finland | May 23, 2018 | Dec 31, 9999 |
| France | May 23, 2018 | Dec 31, 9999 |
| Croatia | May 23, 2018 | Dec 31, 9999 |
| Hungary | May 23, 2018 | Dec 31, 9999 |
| Ireland | May 23, 2018 | Dec 31, 9999 |
| Iceland | May 23, 2018 | Dec 31, 9999 |
| Italy | May 23, 2018 | Dec 31, 9999 |
| Lithuania | May 23, 2018 | Dec 31, 9999 |
| Luxembourg | May 23, 2018 | Dec 31, 9999 |
| Latvia | May 23, 2018 | Dec 31, 9999 |
| Netherlands | May 23, 2018 | Dec 31, 9999 |
| Norway | May 23, 2018 | Dec 31, 9999 |
| Poland | May 23, 2018 | Dec 31, 9999 |
| Portugal | May 23, 2018 | Dec 31, 9999 |
| Romania | May 23, 2018 | Dec 31, 9999 |
| Sweden | May 23, 2018 | Dec 31, 9999 |
| Slovenia | May 23, 2018 | Dec 31, 9999 |
| Slovakia | May 23, 2018 | Dec 31, 9999 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
00606959412958Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
0606959BM224LU1120747UDI 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.
Z1203019080VARIOUS INSTRUMENTS FOR ANAESTHESIA AND PULMONARY VENTILATION SUPPORT - HARDWARE ACCESSORIESB-00606959040502On the marketDreamStation Roll Stand0606959BM136LWOn the marketDreamStation Serial Accessory0606959BM218LZOn the marketDreamStation SpO2 Connection Module0606959BM218LZOn the marketDreamStation Travel Kit, 65W P/S, EUB-00606959413665On the marketDreamStation Wi-Fi Accessory EU, w/PRI0606959BM218LZOn 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.