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Centricity High Acuity Anesthesia

EUDAMED

Class IIa (EU MDR)

Ref K1900A, K1900AA, K1900EGED, K1900EJED, K1900EMED, K1900EPED, K1900ERED, K1900ETEDModel version 5.8

by GE Healthcare Finland Oy

Identity

Device Name
Centricity High Acuity Anesthesia EUDAMED
Model / Reference
version 5.8 EUDAMED
K1900A, K1900AA, K1900EGED, K1900EJED, K1900EMED, K1900EPED, K1900ERED, K1900ETED EUDAMED

Identifiers

Primary DI / UDI-DI
00195278463531 EUDAMED
Basic UDI-DI
8406821BUG00250H5 EUDAMED
EMDN Code
Z1203020282 MULTI-PARAMETER MONITORS - SOFTWARE ACCESSORIES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Special Device Type
Software EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Centricity High Acuity Anesthesia by GE Healthcare Finland Oy — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
FI-MF-000001176

Sources (2)

  • EUDAMED 2f03f3a0-9c80-4ec1-85b1-65e4a94a036b 61 fields · synced Oct 8, 2026
  • EUDAMED 2f03f3a0-9c80-4ec1-85b1-65e4a94a036b-1 61 fields · synced Jun 10, 2026