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Centricity™ High Acuity Anesthesia
EUDAMEDClass I (EU MDR)
Ref K1900EAEDModel Centricity™ High Acuity Anesthesia 5.6
Identity
- Device Name
- Centricity™ High Acuity Anesthesia EUDAMED
- Model / Reference
- Centricity™ High Acuity Anesthesia 5.6 EUDAMEDK1900EAED EUDAMED
Identifiers
- Primary DI / UDI-DI
- 00195278210906 EUDAMED
- Basic UDI-DI
- B-00195278210906 EUDAMED
- EMDN Code
- Z1203020282 MULTI-PARAMETER MONITORS - SOFTWARE ACCESSORIES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Special Device Type
- -1192 EUDAMED
- Market of Registration
- Finland EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
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 I — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-00195278210906 | Class I | Active |
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Manufacturer
- Manufacturer
- GE Healthcare Finland Oy
- EUDAMED SRN
- FI-MF-000001176
Sources (1)
- EUDAMED c85e4bd3-03c7-486c-8d4f-58345782c712 61 fields · synced Jun 18, 2026