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Benda premifistola elastica

EUDAMED

Class I (EU MDR)

Ref DR 9/1C/10Model Dispositivi PremifistolaRef DR 9/1

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

Identity

Trade Name
Benda premifistola elastica EUDAMED
Device Name
Bende Premifistola EUDAMED
Model / Reference
Dispositivi Premifistola EUDAMED
DR 9/1C/10 EUDAMED
DR 9/1 EUDAMED

Identifiers

Primary DI / UDI-DI
08059591525265 EUDAMED
08059591521472 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 elastica 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 2cfeff07-583d-410c-b771-f16e987c940d 61 fields · synced Jul 30, 2026
  • EUDAMED 75789e00-3fca-4b85-9434-b81dac45409d 61 fields · synced May 16, 2026