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Resorcell

EUDAMED

Class III (EU MDR)

Ref 10134Model Resorcell, 2g

by BIOSTER, a.s.

Identity

Trade Name
Resorcell EUDAMED
Device Name
Haemostatic powder EUDAMED
Model / Reference
Resorcell, 2g EUDAMED
10134 EUDAMED

Identifiers

Primary DI / UDI-DI
D-CZMF00001161510134JL EUDAMED
Basic UDI-DI
B-CZMF00001161510134JL EUDAMED
EMDN Code
M040501 POLYSACCHARIDE HAEMOSTATIC DRESSINGS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Czechia 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

Resorcell by BIOSTER, a.s. — 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
BIOSTER, a.s.
EUDAMED SRN
CZ-MF-000011615

Sources (1)

  • EUDAMED d183f3e6-3d58-4e6d-96cc-cdf6bb6cf2b7 61 fields · synced Jul 14, 2026