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Pressure Bag

EUDAMED

Class I (EU MDR)

Ref T1000Model TWINFUSER

by Intersurgical SpA

Identity

Device Name
PRESSURE BAG EUDAMED
Model / Reference
TWINFUSER EUDAMED
T1000 EUDAMED

Identifiers

Primary DI / UDI-DI
08058323016958 EUDAMED
Basic UDI-DI
80583230DCPREMISACCAHB EUDAMED
Direct Marketing DI
08058323016958 EUDAMED
EMDN Code
A99 DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - OTHER EUDAMED

Classification

Device Class
Class I 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

Yes

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

Pressure Bag by Intersurgical SpA — 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
Intersurgical SpA
EUDAMED SRN
IT-MF-000010729

Sources (1)

  • EUDAMED 5033167b-434a-42fd-8ce5-d5ddcb8271c4 61 fields · synced Aug 1, 2026