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Leucocyte Alkaline Phosphatase Kit

EUDAMEDFDA UDI

Class A (EU MDR)

Ref 86R-1KTModel 86

by Sigma-Aldrich Corporation

Identity

Trade Name
LEUCOCYTE ALKALINE PHOSPHATASE KIT EUDAMED
ALKALINE PHOSPHATASE FDA UDI
Generic Name
Alkaline phosphatase (ALP) isoenzyme IVD, reagent FDA UDI
Device Name
LEUCOCYTE ALKALINE PHOSPHATASE KIT EUDAMED
Model / Reference
86 EUDAMED
86R-1KT EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
04061838261182 EUDAMEDFDA UDI
Basic UDI-DI
04061886CR6A EUDAMED
FDA Product Code
JCJ FDA UDI
EMDN Code
W0103010301 HISTO / CYTO STAINS EUDAMED
GMDN Term
Alkaline phosphatase (ALP) isoenzyme IVD, reagent FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
864.7660 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Leucocyte Alkaline Phosphatase Kit by Sigma-Aldrich Corporation — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

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

Sources (2)

  • EUDAMED fe0d4b20-d947-4aa9-808f-bac1ce1b8cbf 61 fields · synced Jun 18, 2026
  • FDA UDI 09f61d60-6193-4b95-bc89-e4fa3df29ed3 33 fields · synced May 29, 2026