← Back to catalogue

Bimboneb

EUDAMED

Class IIa (EU MDR)

Ref 400151

by Air Liquide Medical Systems S.r.l.

Identity

Trade Name
Bimboneb EUDAMED
Device Name
Bimboneb EUDAMED
Model / Reference
400151 EUDAMED

Identifiers

Primary DI / UDI-DI
08015662001519 EUDAMED
Basic UDI-DI
8015662BIMBONEBVF EUDAMED
EMDN Code
Z12159002 AEROSOL EQUIPMENT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Bimboneb by Air Liquide Medical Systems S.r.l. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
IT-MF-000015627

Sources (1)

  • EUDAMED 8573c0f3-5460-488a-9225-eb4a19fabf44 61 fields · synced Jun 18, 2026