← Back to catalogue

Neopump-R

EUDAMED

Class IIb (EU MDR)

Ref NBF0800RNFModel NHS

by Adria Med S.r.l.

Identity

Trade Name
NEOPUMP-R EUDAMED
Device Name
NEOPUMP-R EUDAMED
Model / Reference
NHS EUDAMED
NBF0800RNF EUDAMED

Identifiers

Primary DI / UDI-DI
08052204713981 EUDAMED
Basic UDI-DI
80522047103EASYNRVE EUDAMED
Direct Marketing DI
08052204713981 EUDAMED
EMDN Code
A05010101 ELASTOMERIC SYSTEMS - FIXED FLOW W/O ADDITIONAL BOLUS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

Yes

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

Neopump-R by Adria Med S.r.l. — Class IIb — 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

Manufacturer
Adria Med S.r.l.
EUDAMED SRN
IT-MF-000020866

Sources (1)

  • EUDAMED 1da6f28c-e04f-4225-af29-2ea9d757524d 61 fields · synced Jun 18, 2026