← Back to catalogue
Leukocyte Acid Phosphatase (trap) Kit
EUDAMEDClass A (EU MDR)
Ref 3872-10MLModel 387
Identity
- Device Name
- LEUKOCYTE ACID PHOSPHATASE (TRAP) KIT EUDAMED
- Model / Reference
- 387 EUDAMED3872-10ML EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04061838202918 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 040618387KB | Class A | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Sigma-Aldrich Corporation
- EUDAMED SRN
- US-MF-000025162
- Authorised Representative
- MDSS GmbH DE-AR-000005430
Sources (1)
- EUDAMED 0182c9a2-e09e-4157-83dc-fd13665fad8b 61 fields · synced Jun 17, 2026