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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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EmbryoViewer version 7 (incl. Guided… — 2 UDI-DI variants, MDR

MD Atlas
Vitrolife A/S

Data from EUDAMED, last updated May 31, 2026

EmbryoViewer version 7 (incl. Guided Annotation)

5712714SWA-01S4

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: Vitrolife A/S

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5712714SWA-01S4
Device name: EmbryoViewer version 7 (incl. Guided Annotation)
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: Feb 12, 2023

Manufacturer & authorised representative

Manufacturer

Name: Vitrolife A/S
SRN: DK-MF-000001892
Country: Denmark
Email: Hwahlgren@vitrolife.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01GBYGNV3XF07N92QF0FBW640B

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

1662205712714676222
1661205712714676123