- Organization name
- UDI-DI code
- Reference / catalog number
FR-MF-000011282Nebulisation filter is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by INOSYSTEMS. Placed on the EU market in Austria. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Mar 20, 2025
376033338_INO_SAMPLINGGQPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)03760333380381
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.
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 14 countries total.
| Country | On market since | Until |
|---|---|---|
| AustriaPrimary placement | Aug 25, 2023 | Aug 25, 2028 |
| Belgium | Aug 25, 2023 | Aug 25, 2028 |
| Germany | Aug 25, 2023 | Aug 25, 2028 |
| Denmark | Aug 25, 2023 | Aug 25, 2028 |
| EL | Aug 25, 2023 | Aug 25, 2028 |
| Spain | Aug 25, 2023 | Aug 25, 2028 |
| France | Aug 25, 2023 | Aug 25, 2028 |
| Ireland | Aug 25, 2023 | Aug 25, 2028 |
| Italy | Aug 25, 2023 | Aug 25, 2028 |
| Netherlands | Aug 25, 2023 | Aug 25, 2028 |
| Norway | Aug 25, 2023 | Aug 25, 2028 |
| Poland | Aug 25, 2023 | Aug 25, 2028 |
| Portugal | Aug 25, 2023 | Aug 25, 2028 |
| Sweden | Aug 25, 2023 | Aug 25, 2028 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
03760333380381Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
376033338_INO_SAMPLINGGQIN000148UDI 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 ACCESSORIESNo 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.
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