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Swelab Alfa ComboPack 200

EUDAMED

Class A (EU MDR)

Ref 1504127

by Boule Medical AB

Identity

Trade Name
Swelab Alfa ComboPack 200 EUDAMED
Device Name
Swelab Alfa reagents EUDAMED
Model / Reference
1504127 EUDAMED

Identifiers

Primary DI / UDI-DI
07350040790304 EUDAMED
Basic UDI-DI
735004079A013YD EUDAMED
EMDN Code
W0103010105 CBC-REAGENTS (CLEANING-/DILUTING-/LYSING-/SHEATH-FLUIDS) EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Sweden EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Swelab Alfa ComboPack 200 by Boule Medical AB — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
Boule Medical AB
EUDAMED SRN
SE-MF-000001911

Sources (1)

  • EUDAMED f7396aca-97a6-4b41-8c4b-5719b9665895 61 fields · synced Jun 18, 2026