Identity
- Trade Name
- AQUIOS PLG Panel 400 Test EUDAMED
- Device Name
- AQUIOS PLG EUDAMED
- Model / Reference
- AQUIOS PLG EUDAMEDB43610 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 15099590663667 EUDAMED
- Basic UDI-DI
- 150995902AQUIOSPLGPANELCT EUDAMED
- EMDN Code
- W0103080101 ANTIBODIES FOR B AND T-CELL SUBTYPING EUDAMED
Classification
- Device Class
- Class C EUDAMED
- Market of Registration
- Ireland EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
Yes
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
AQUIOS PLG Panel 400 Test by Beckman Coulter Ireland Inc. — Class C — 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 | 150995902AQUIOSPLGPANELCT | Class C | Active |
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Manufacturer
- Manufacturer
- Beckman Coulter Ireland Inc.
- EUDAMED SRN
- IE-MF-000000887
Sources (1)
- EUDAMED af1967d5-9606-48b8-a42f-8f1fd43b4b7d 61 fields · synced Jul 11, 2026