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Bende premifistola elastiche

EUDAMED

Class I (EU MDR)

Ref DR BB/2Model Dispositivi PremifistolaRef DR 9/2Ref DR 8/2

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

Identity

Trade Name
Bende premifistola elastiche EUDAMED
Device Name
Bende Premifistola EUDAMED
Model / Reference
Dispositivi Premifistola EUDAMED
DR BB/2 EUDAMED
DR 9/2 EUDAMED
DR 8/2 EUDAMED

Identifiers

Primary DI / UDI-DI
08059591522103 EUDAMED
08059591521298 EUDAMED
08059591523483 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

Bende premifistola elastiche 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 (3)

  • EUDAMED 656d548f-04ae-4330-b9c1-bab13ba5d726 61 fields · synced Aug 3, 2026
  • EUDAMED bebc0da1-03ba-4836-b726-5122438dfe39 61 fields · synced May 17, 2026
  • EUDAMED 889504ea-b819-4e95-afb3-11b3852eaeab 61 fields · synced May 19, 2026