← Back to catalogue

Solite Pro Bed

EUDAMED

Class I (EU MDR)

Ref SOLITE/PRO

by Drive DeVilbiss Healthcare Limited

Identity

Trade Name
Solite Pro Bed EUDAMED
Device Name
Solite Pro EUDAMED
Model / Reference
SOLITE/PRO EUDAMED

Identifiers

Primary DI / UDI-DI
05055154400843 EUDAMED
Basic UDI-DI
50551544ABD002XJ EUDAMED
Direct Marketing DI
05055154400843 EUDAMED
EMDN Code
V08060101 HOSPITAL/HOME CARE ELECTRIC MEDICAL BEDS 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

Category: Basic electric hospital bed

Solite Pro Bed by Drive DeVilbiss Healthcare Limited — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Basic electric hospital bed.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
GB-MF-000012818
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED 37ea8005-d14b-4b39-b56e-a5f8f6e0ef6d 61 fields · synced Jun 19, 2026