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Minstrel

EUDAMED

Class I (EU MDR)

Ref HMA0007-UKModel KHA1010Ref HMA0006

by ArjoHuntleigh AB

Identity

Trade Name
Minstrel EUDAMED
Device Name
Tenor EUDAMED
Model / Reference
KHA1010 EUDAMED
HMA0007-UK EUDAMED
HMA0006 EUDAMED

Identifiers

Primary DI / UDI-DI
05055982787635 EUDAMED
05055982787581 EUDAMED
Basic UDI-DI
5060693520082W3 EUDAMED
EMDN Code
V0805030102 ELECTRIC MOBILE LIFTS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland EUDAMED
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

Yes

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 (2)

  • EUDAMED b99c6ab3-66f6-4483-8a5a-1fd155fef323 61 fields · synced Jul 21, 2026
  • EUDAMED b5f3eca7-f503-4868-a6be-6236d7d89227 61 fields · synced May 19, 2026