← Back to catalogue
Centricity High Acuity
EUDAMEDClass IIa (EU MDR)
Ref K1900CYEDModel Centricity High Acuity Clinical Notification Module 5.5
Identity
- Trade Name
- Centricity High Acuity EUDAMED
- Device Name
- Centricity High Acuity Clinical Notification Module EUDAMED
- Model / Reference
- Centricity High Acuity Clinical Notification Module 5.5 EUDAMEDK1900CYED EUDAMED
Identifiers
- Primary DI / UDI-DI
- 00840682143813 EUDAMED
- Basic UDI-DI
- B-00840682143813 EUDAMED
- EMDN Code
- Z1203020282 MULTI-PARAMETER MONITORS - SOFTWARE ACCESSORIES EUDAMED
Classification
- Device Class
- Class IIa 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 by GE Healthcare Finland Oy — Class IIa — 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-00840682143813 | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- GE Healthcare Finland Oy
- EUDAMED SRN
- FI-MF-000001176
Sources (1)
- EUDAMED 703096b9-637f-411c-b568-391019ac4bbf 61 fields · synced Oct 5, 2026