← Back to catalogue

Enterprise 9000x

EUDAMED

Class I (EU MDR)

Ref 9X22CZ101BFABAModel 9X21AE111BFCSA

by ArjoHuntleigh AB

Identity

Trade Name
ENTERPRISE 9000X EUDAMED
Device Name
ENTERPRISE 9000X EUDAMED
Model / Reference
9X21AE111BFCSA EUDAMED
9X22CZ101BFABA EUDAMED

Identifiers

Primary DI / UDI-DI
05056097300559 EUDAMED
Basic UDI-DI
5060693520075W6 EUDAMED
EMDN Code
V08060105 ELECTRIC MEDICAL BEDS WITH WEIGHING SYSTEM EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Enterprise 9000x by Arjohuntleigh AB — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

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

Manufacturer
ArjoHuntleigh AB
EUDAMED SRN
SE-MF-000000696

Sources (1)

  • EUDAMED c8d54769-315c-4ffd-bd41-a88168c2afc6 61 fields · synced Jun 19, 2026