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Embryoaid

EUDAMED

Class I (EU MDR)

Ref EMBRYOAID 2.0Ref EMBRYOAID

by MIM Fertility Sp. z o.o.

Identity

Trade Name
EMBRYOAID EUDAMED
Device Name
EMBRYOAID EUDAMED
Model / Reference
EMBRYOAID 2.0 EUDAMED
EMBRYOAID EUDAMED

Identifiers

Primary DI / UDI-DI
05905090198932 EUDAMED
05905090198901 EUDAMED
Basic UDI-DI
59050901989fertilityVS EUDAMED
EMDN Code
U080299 DEVICES FOR ASSISTED REPRODUCTION - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Special Device Type
Software EUDAMED
Market of Registration
Poland 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

Category: Assisted reproduction vitrification carrier

Embryoaid by MIM Fertility Sp. z o.o. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Assisted reproduction vitrification carrier.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
PL-MF-000030821

Sources (2)

  • EUDAMED a12918b0-c1fe-4b99-a47e-09eb0b845da0 61 fields · synced Jul 9, 2026
  • EUDAMED c4ad1797-6836-4fff-8ea9-814b6d5ed6b3 61 fields · synced May 18, 2026