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BloodSTOP iX

EUDAMED

Class III (EU MDR)

Ref BS-iX22

by LifeScience PLUS, Inc.

Identity

Trade Name
BloodSTOP iX EUDAMED
Device Name
BloodSTOP iX EUDAMED
Model / Reference
BS-iX22 EUDAMED

Identifiers

Primary DI / UDI-DI
D-USMF000004095IX22EULF EUDAMED
Basic UDI-DI
B-USMF000004095IX22EULF EUDAMED
EMDN Code
M040501 POLYSACCHARIDE HAEMOSTATIC DRESSINGS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Greece 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

BloodSTOP iX by LifeScience 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

EUDAMED SRN
US-MF-000004095
Authorised Representative
Wellkang Ltd XI-AR-000001836

Sources (1)

  • EUDAMED 21c149f1-407a-477e-abc2-2b97d72bb6c1 61 fields · synced Jun 9, 2026