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Diacan®

EUDAMED

Class IIa (EU MDR)

Ref 7021432-01Ref 7021625-01Ref 7021632-01

by B. Braun Avitum AG

Identity

Trade Name
Diacan® EUDAMED
Device Name
Diacan Flex EUDAMED
Model / Reference
7021432-01 EUDAMED
7021625-01 EUDAMED
7021632-01 EUDAMED

Identifiers

Primary DI / UDI-DI
04046955134809 EUDAMED
04046955343799 EUDAMED
04046955138203 EUDAMED
Basic UDI-DI
40392390000016072J EUDAMED
EMDN Code
A010499 DIALYSIS NEEDLES - OTHER EUDAMED

Classification

Device Class
Class IIa 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

Diacan® by B.Braun Avitum AG — Class IIa — 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 (3)

  • EUDAMED 53852a3a-2aef-44a7-abdc-4868f681f73f 61 fields · synced Jul 25, 2026
  • EUDAMED e0fda136-13a0-4524-80d7-dbcdc18c12af 61 fields · synced May 17, 2026
  • EUDAMED fb385f29-56dc-4473-a89b-efdb36bfda02 61 fields · synced May 18, 2026