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Diversi-Foam

EUDAMED

Class IIa (EU MDR)

Ref UPRA3678H-4Model Diversi-Foam II

by Ultimate Healthcare

Identity

Trade Name
Diversi-Foam EUDAMED
Device Name
Diversi-Foam II Hybrid Replacement Mattress & Pump EUDAMED
Model / Reference
Diversi-Foam II EUDAMED
UPRA3678H-4 EUDAMED

Identifiers

Primary DI / UDI-DI
05056019108010 EUDAMED
Basic UDI-DI
B-05056019108010 EUDAMED
EMDN Code
V080701 ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES EUDAMED

Classification

Device Class
Class IIa 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

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

Diversi-Foam by Ultimate Healthcare — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Ultimate Healthcare
EUDAMED SRN
GB-MF-000021288
Authorised Representative
CS Life Sciences Europe Ltd IE-AR-000004113

Sources (1)

  • EUDAMED 817acae0-2d24-4ee6-818f-f8accadc9b6f 61 fields · synced Jun 18, 2026