- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Jan 18, 2023
B-E3091601ASF0MASTER FLUX PLUS A MURO AFNOR is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Tecno-Gaz S.p.A. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
E3091601ASF01601ASFE3091601ASF0
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA / IFA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z120309MEDICAL/MEDICINAL GAS PIPELINE SYSTEMS AND RELATED ACCESSORIES1 warning recorded — scroll inside the panel to see all entries.
Primary placement in Italy; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Jan 1, 1995 | Still on market |
IT-MF-000010075991/MDDSterile
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 →No certificate specifically references this device's Basic UDI-DI.
B-E3091600ASD0On the marketMASTER FLUX PLUS A MOBILE UNIB-E3091600AS0On the marketMASTER FLUX PLUS A MUROB-E309MF008ZMF0On the marketMASTER FLUX PLUS A MURO AFNOR - UNIB-E309MF010ZMF0On the marketMASTER FLUX PLUS A MURO DINB-E3091601ASD0On the marketMASTER FLUX PLUS A MURO UNIB-E3091601AS0On the marketNo 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.