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Swelab AlfaLyse, RFID

EUDAMED

Class A (EU MDR)

Ref 1504463

by Boule Medical AB

Identity

Trade Name
Swelab AlfaLyse, RFID EUDAMED
Device Name
Swelab Alfa reagents EUDAMED
Model / Reference
1504463 EUDAMED

Identifiers

Primary DI / UDI-DI
07350040796313 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 AlfaLyse, RFID 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 e9f7e67b-4efc-4f0f-b8d3-f99788b1cd3e 61 fields · synced Jun 17, 2026