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Miranti

EUDAMED

Class I (EU MDR)

Ref CEB8302-01Model CDB6021-01

by ArjoHuntleigh AB

Identity

Trade Name
Miranti EUDAMED
Device Name
CALYPSO EUDAMED
Model / Reference
CDB6021-01 EUDAMED
CEB8302-01 EUDAMED

Identifiers

Primary DI / UDI-DI
05055982796347 EUDAMED
Basic UDI-DI
5060693520068W9 EUDAMED
EMDN Code
V08050399 PATIENT TRANSFER LIFTS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Miranti 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 68ff37c8-ed40-4f6b-b07d-898df9eb9cf9 61 fields · synced Jun 19, 2026