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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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Embryo Biopsy Kit — 2 UDI-DI variants, IVDR (JUNO GENETICS ESPAÑA)

MD Atlas
JUNO GENETICS ESPAÑA

Data from EUDAMED, last updated May 23, 2026

Embryo Biopsy Kit

8437026899EBKE9

2 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: JUNO GENETICS ESPAÑA

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 8437026899EBKE9
Device name: Embryo Biopsy Kit
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jul 10, 2025

Manufacturer & authorised representative

Manufacturer

Name: JUNO GENETICS ESPAÑA
SRN: ES-MF-000045150
Country: Spain
Email: supportspain@junogenetics.com
Phone: +34 960694800

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JEZKXX5GRR3AX5ZN70BVQ3MV

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

EMBRYO BIOPSY KIT (10ud)08437026899004
EMBRYO BIOPSY KIT (60ud)08437026899028