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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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EMBRYOAID — 2 UDI-DI variants, MDR (MIM Fertility Sp. z o.o.)

MD Atlas
MIM Fertility Sp. z o.o.

Data from EUDAMED, last updated May 30, 2026

EMBRYOAID

59050901989fertilityVS

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: MIM Fertility Sp. z o.o.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 59050901989fertilityVS
Device name: EMBRYOAID
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Special device type: refdata.special-mdr-device-type.software
Version date: Jan 26, 2023

Manufacturer & authorised representative

Manufacturer

Name: MIM Fertility Sp. z o.o.
SRN: PL-MF-000030821
Country: Poland
Email: paulina.stefanowicz@mimfertility.ai
Phone: +48503038948

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01GM8NFKFESTESFGQGBG565PWX

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

EMBRYOAID 2.005905090198932
EMBRYOAID05905090198901