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Traumastem P

EUDAMED

Class III (EU MDR)

Ref 60105Model Traumastem P, 1g

by BIOSTER, a.s.

Identity

Trade Name
Traumastem P EUDAMED
Device Name
Haemostatic powder EUDAMED
Model / Reference
Traumastem P, 1g EUDAMED
60105 EUDAMED

Identifiers

Primary DI / UDI-DI
D-CZMF00001161560105L4 EUDAMED
Basic UDI-DI
B-CZMF00001161560105L4 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

Traumastem P 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 dd737b5b-d021-45d7-8873-cd6846ddd820 61 fields · synced Jun 19, 2026