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EndoClot®

EUDAMED

Class III (EU MDR)

Ref EPK2303

by EndoClot Plus, Inc.

Identity

Trade Name
EndoClot® EUDAMED
Device Name
EndoClot® Polysaccharide Hemostatic System EUDAMED
Model / Reference
EPK2303 EUDAMED

Identifiers

Primary DI / UDI-DI
00856886003051 EUDAMED
10856886003058 EUDAMED
Basic UDI-DI
B-00856886003051 EUDAMED
B-10856886003058 EUDAMED
EMDN Code
M040501 POLYSACCHARIDE HAEMOSTATIC DRESSINGS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

EndoClot® by EndoClot Plus, Inc. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
EndoClot Plus, Inc.
EUDAMED SRN
US-MF-000003502
Authorised Representative
ClotPlus Limited IE-AR-000002109

Sources (2)

  • EUDAMED 45e30718-a419-4035-a159-998860b9dde0 61 fields · synced Jul 30, 2026
  • EUDAMED 9a7a15e5-0e47-4c40-bf14-c9b174af85ab 61 fields · synced May 17, 2026