- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Jun 29, 2026
570748030100600107HVivaSight™ 2 DLT Kit 41 Fr - LEFT is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Ambu A/S. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
057074801457994124110001 packaging level registered — each level carries its own UDI-DI.
05707480145799× 1 unitBase unit05707480145805× 5 units(01)05707480145799
European Medical Device Nomenclature — the EU product classification assigned to this device.
R01040202ENDOBRONCHIAL OROPHARYNGEAL TUBES, LEFTDK-PR-000001946The 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 →No certificate specifically references this device's Basic UDI-DI.
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 →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.570748030100600107HOn the marketVivaSight™ 2 DLT Kit 37 Fr - LEFT570748030100600107HOn the marketVivaSight™ 2 DLT Kit 39 Fr - LEFT570748030100600107HOn the marketVivaSight™ 2 SLT + EBB Kit - 7.0 mm, 9 Fr570748030101072007LOn the marketVivaSight™ 2 SLT + EBB Kit - 7.5 mm, 9 Fr570748030101072007LOn the marketVivaSight™ 2 SLT + EBB Kit - 8.0 mm, 9 Fr570748030101072007LOn the market