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Diacap®

EUDAMED

Class IIb (EU MDR)

Ref 720AT19

by B. Braun Avitum AG

Identity

Trade Name
Diacap® EUDAMED
Device Name
Diacap Acute Pro EUDAMED
Model / Reference
720AT19 EUDAMED

Identifiers

Primary DI / UDI-DI
04046955764570 EUDAMED
Basic UDI-DI
40392390000016192R EUDAMED
EMDN Code
F01060303 DIALYSERS - UFC > 35 ml/h/mmHg, SYNTHETIC MEMBRANES EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany 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

Diacap® by B.Braun Avitum AG — Class IIb — 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
B. Braun Avitum AG
EUDAMED SRN
DE-MF-000005127

Sources (1)

  • EUDAMED b610aa97-4fc6-4e37-a639-178da1ba9391 61 fields · synced May 23, 2026