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EUDAMED last updated this device on Jun 16, 2026
B-A577EBbuonerbe® MICROCLISMI ADULTI is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Industria Farmaceutica NOVA ARGENTIA S.r.l.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
D-A577EB577IT-MF-00002891326980D-A577EB
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
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 Italy; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Jan 21, 2022 | Dec 31, 2028 |
| Croatia | Apr 18, 2023 | Dec 31, 2028 |
European Medical Device Nomenclature — the EU product classification assigned to this device.
G99GASTROINTESTINAL DEVICES - OTHERG05TOPICAL ANORECTAL ADMINISTERED GASTRO-INTESTINAL SYSTEM DEVICESPrimary 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 →B-BPF_I01708901F9On the marketBeneffèct NaturalGo MICROCLISMI CON PROPOLAX® ADULTIB-PF_I0171890193On the marketBensania Hemosoft trastornos hemorroidales 30 gB-305002686LOn the marketbuonerbe® MICROCLISMI PEDIATRICO 1+B-B576EGOn the marketCrème Hémorroïde Biogaran conseil®B-3050021763On the marketDr. Max Hemo HA Single-dose tubesB-5500250X3On 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.No certificate specifically references this device's Basic UDI-DI.