← Back to catalogue
Artemis II
EUDAMEDClass I (EU MDR)
Ref DYN/DIG/ARTEMIS/2Model Artemis II dynamic system
Identity
- Trade Name
- Artemis II EUDAMED
- Device Name
- Artemis II dynamic mattress system EUDAMED
- Model / Reference
- Artemis II dynamic system EUDAMEDDYN/DIG/ARTEMIS/2 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05055785718409 EUDAMED
- Basic UDI-DI
- 50557857DPC013FD EUDAMED
- EMDN Code
- V080701 ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Northern Ireland 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
Artemis II by Drive DeVilbiss Healthcare Limited — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 50557857DPC013FD | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Drive DeVilbiss Healthcare Limited
- EUDAMED SRN
- GB-MF-000012818
- Authorised Representative
- Advena Limited MT-AR-000000234
Sources (1)
- EUDAMED 141e2332-615c-4b2e-add1-912dcd899d0e 61 fields · synced Jun 19, 2026