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Allmed SafeFlow

EUDAMED

Class IIa (EU MDR)

Ref SFL 22

by Allmed Medical GmbH

Identity

Trade Name
Allmed SafeFlow EUDAMED
Device Name
Bacterial and Endotoxin Retention Filter EUDAMED
Model / Reference
SFL 22 EUDAMED

Identifiers

Primary DI / UDI-DI
04260157725515 EUDAMED
Basic UDI-DI
426015772SAFEFLOWEOXQ EUDAMED
Direct Marketing DI
04260157725515 EUDAMED
EMDN Code
F01080201 ENDOTOXIN REMOVAL FILTERS 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

Allmed SafeFlow by Allmed Medical GmbH — 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
Allmed Medical GmbH
EUDAMED SRN
DE-MF-000007862

Sources (1)

  • EUDAMED 4ffd6d5b-34a9-4a67-8416-30591de2eb04 61 fields · synced Jun 19, 2026