- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Jul 24, 2026
843603552ACAP00101ELCabina audiométrica S40 F is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by SIBEL SAU. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0843603552373307107(01)08436035523733
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12149002AUDIOMETRIC CHAMBERSPrimary placement in Spain; available across 3 countries total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | Jun 23, 2026 | Still on market |
| France | Jun 23, 2026 | Still on market |
| Portugal | Jun 23, 2026 | Still on market |
ES-MF-000000287The 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.
View in glossary →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.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →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.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Certificate health across this manufacturer's portfolio.
2024 CR 0025SupplementedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
No certificate specifically references this device's Basic UDI-DI.
843603552ACAP00101ELOn the marketCabina audiométrica S40 D843603552ACAP00101ELOn the marketCabina audiométrica S40 E843603552ACAP00101ELOn the marketDatospir Aira D843603552AESP00302RQOn the marketDatospir Aira F843603552AESP00302RQOn the marketDatospir Aira T843603552AESP00302RQOn the market