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Minstrel

EUDAMED

Class I (EU MDR)

Ref HMA0001Model HEB0000

by ArjoHuntleigh AB

Identity

Trade Name
Minstrel EUDAMED
Device Name
SARA FLEX EUDAMED
Model / Reference
HEB0000 EUDAMED
HMA0001 EUDAMED

Identifiers

Primary DI / UDI-DI
05055982787543 EUDAMED
Basic UDI-DI
5060693520112VK EUDAMED
EMDN Code
V0805030102 ELECTRIC MOBILE LIFTS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

Minstrel 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

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Manufacturer

Manufacturer
ArjoHuntleigh AB
EUDAMED SRN
SE-MF-000000696

Sources (1)

  • EUDAMED aba153c3-e844-46e6-953a-8481cca2c412 61 fields · synced Jun 19, 2026