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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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Organization name
UDI-DI code
Reference / catalog number

DAVITRI DISH — Class IIa MDR by OVERTURE LIFE, S.L.

MD Atlas
OVERTURE LIFE, S.L.

EUDAMED last updated this device on Nov 28, 2025

DAVITRI DISH

8437021820DVDISH8C

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: OVERTURE LIFE, S.L.
UDI-DI code: 08437021820010
Reference / catalog number: DD-AS-0001

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Manufacturer information

Organization name: OVERTURE LIFE, S.L.
SRN: ES-MF-000047403
Manufacturer status: Active

Critical warnings

5 warnings recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW032
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement		Still on market

Device identification

Trade name: DAVITRI DISH
UDI-DI code: 08437021820010
Basic UDI-DI: 8437021820DVDISH8C
Reference / catalog number: DD-AS-0001
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: DaVitri Dish is intended for preparation of vitrification of human oocytes. This Dish must be used together with DaVitri Station. For Use Only with DaVitri Station. Contents: 1 DaVitri Dish. For Use Only With Kitazato Media - VT601 - VT601US. Made in Spain
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12080285GYNAECOLOGY AND FERTILITY TREATMENT INSTRUMENTS - CONSUMABLES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

DS-AS-00018437021820DVSTATIONTWOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.