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MIRI® Humidity

EUDAMED

Class IIa (EU MDR)

Ref MRI-6A10-H-8Model MIRI®

by Esco Medical Technologies, UAB

Identity

Trade Name
MIRI® Humidity EUDAMED
Device Name
Multiroom IVF incubator EUDAMED
Model / Reference
MIRI® EUDAMED
MRI-6A10-H-8 EUDAMED

Identifiers

Primary DI / UDI-DI
04779041940236 EUDAMED
Basic UDI-DI
477904194MIRIFAMYP EUDAMED
Direct Marketing DI
04779041940236 EUDAMED
EMDN Code
Z12080299 GYNAECOLOGY AND FERTILITY TREATMENT INSTRUMENTS - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Lithuania 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

MIRI® Humidity by Esco Medical Technologies, UAB — Class IIa — 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

EUDAMED SRN
LT-MF-000010902

Sources (1)

  • EUDAMED 85b67d42-0971-48ad-b7c6-b22347928207 61 fields · synced Jul 16, 2026