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Benda premifistola coesiva

EUDAMED

Class I (EU MDR)

Ref IB0786Model Dispositivi PremifistolaRef DR 10-1A-10

by D.r.m. S.r.l.

Identity

Trade Name
Benda premifistola coesiva EUDAMED
Device Name
Bende Premifistola EUDAMED
Model / Reference
Dispositivi Premifistola EUDAMED
IB0786 EUDAMED
DR 10-1A-10 EUDAMED

Identifiers

Primary DI / UDI-DI
08059591520048 EUDAMED
08059591522004 EUDAMED
Basic UDI-DI
805959152PREMN4 EUDAMED
EMDN Code
M030404 DIALYSIS FISTULA, BANDAGES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Benda premifistola coesiva by D.r.m. S.r.l. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
D.r.m. S.r.l.
EUDAMED SRN
IT-MF-000027115

Sources (2)

  • EUDAMED 6b9a8745-6118-4791-aa7f-e994c41651ff 61 fields · synced Jul 25, 2026
  • EUDAMED f66917aa-de4d-4682-91c5-6521d210a0c6 61 fields · synced May 18, 2026