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AKUTOL™ STOP sprej

EUDAMED

Class IIa (EU MDR)

Ref Z400000Ref Z070000Ref SZ58

by AVEFLOR, a.s.

Identity

Trade Name
AKUTOL™ STOP sprej EUDAMED
Device Name
AKUTOL STOP™ spray EUDAMED
Model / Reference
Z400000 EUDAMED
Z070000 EUDAMED
SZ58 EUDAMED

Identifiers

Primary DI / UDI-DI
08594013704793 EUDAMED
08594013701938 EUDAMED
08594013704199 EUDAMED
Basic UDI-DI
859401370Z07NG EUDAMED
EMDN Code
M040599 HAEMOSTATIC DRESSINGS - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Czechia EUDAMED

Clinical & Handling

Sterile

No

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

AKUTOL™ STOP sprej by AVEFLOR, a.s. — 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
AVEFLOR, a.s.
EUDAMED SRN
CZ-MF-000003103

Sources (3)

  • EUDAMED b169d248-6ba4-4b70-bc13-04735ea6cfbf 61 fields · synced Jul 21, 2026
  • EUDAMED 251eefd4-2871-4a3e-9e22-23243032cfd6 61 fields · synced May 18, 2026
  • EUDAMED a47959ee-f210-4d32-a0cf-1ba4e53d8c27 61 fields · synced May 18, 2026