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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

19310/0147 — Class IIa MDR by Vitrolife GmbH

MD Atlas
Vitrolife GmbH

EUDAMED last updated this device on Apr 16, 2026

19310/0147

4260604170045N

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Vitrolife GmbH
UDI-DI code: 04260604170042
Reference / catalog number: 19310/0147

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Manufacturer information

Organization name: Vitrolife GmbH
SRN: DE-MF-000007378
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Apr 14, 2021	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260604170042
Basic UDI-DI: 4260604170045N
Reference / catalog number: 19310/0147
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: —
Additional information URL: https://www.vitrolife.com/products/laser-imaging-systems/octax-laser--imaging-systems/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12080205OOCYTE LASER DRILLS

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

19310/0148M4260604170015GOn the market 19310/01464260604170025JOn 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.