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Leukocyte Acid Phosphatase (trap) Kit

EUDAMED

Class A (EU MDR)

Ref 387A-1KTModel 387

by Sigma-Aldrich Corporation

Identity

Trade Name
LEUKOCYTE ACID PHOSPHATASE (TRAP) KIT EUDAMED
Leukocyte Acid Phosphatase (TRAP) Kit 387 EUDAMED
Device Name
LEUKOCYTE ACID PHOSPHATASE (TRAP) KIT EUDAMED
Leukocyte Acid Phosphatase (TRAP) Kit 387 EUDAMED
Model / Reference
387 EUDAMED
387A-1KT EUDAMED

Identifiers

Primary DI / UDI-DI
04061831967975 EUDAMED
Basic UDI-DI
040618387KB EUDAMED
EMDN Code
W0103010301 HISTO / CYTO STAINS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany 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

Leukocyte Acid Phosphatase (trap) Kit by Sigma-Aldrich Corporation — 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

EUDAMED SRN
US-MF-000025162
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (2)

  • EUDAMED 71f3ae3d-7170-4c5a-aeb1-a546424428c3 61 fields · synced Jun 19, 2026
  • EUDAMED 9ac2c503-4bc3-46eb-ac6f-66d5034eb408 61 fields · synced Jun 19, 2026