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Glissando RS20

EUDAMED

Class A (EU MDR)

Ref GLISS-RS20-IVDModel A002HR-RS20-IVD

by Objective Imaging Ltd

Identity

Trade Name
Glissando RS20 EUDAMED
Device Name
Glissando RS20 EUDAMED
Model / Reference
A002HR-RS20-IVD EUDAMED
GLISS-RS20-IVD EUDAMED

Identifiers

Primary DI / UDI-DI
05060905850068 EUDAMED
Basic UDI-DI
506090585AAA002S5 EUDAMED
Direct Marketing DI
05060905850068 EUDAMED
EMDN Code
W0202050304 DIGITAL LABORATORY MICROSCOPES EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

Yes

EUDAMED

Glissando RS20 by Objective Imaging Ltd — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
GB-MF-000016742
Authorised Representative
Acorn Regulatory Consultancy Services Ltd IE-AR-000000592

Sources (1)

  • EUDAMED ac8045c3-606e-4c61-accc-95e5b0eeec8d 61 fields · synced Jul 8, 2026