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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

CBC EVA1030 — Class IIb MDR by Cord Blood Center…

MD Atlas
Cord Blood Center Laboratories, s.r.o.

EUDAMED last updated this device on Apr 14, 2026

CBC EVA1030

8588010018CBCEVA5K

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Cord Blood Center Laboratories, s.r.o.
UDI-DI code: 08588010018045
Reference / catalog number: CBC EVA1030

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View device family (Basic UDI)

Manufacturer information

Organization name: Cord Blood Center Laboratories, s.r.o.
SRN: SK-MF-000016461
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Slovakia; available across 1 country total.

Country	On market since	Until
SlovakiaPrimary placement	Mar 16, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08588010018045
Basic UDI-DI: 8588010018CBCEVA5K
Reference / catalog number: CBC EVA1030
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: EVA Cryopreservation bag je určený na dlhodobé uchovávanie buniek, tkanív alebo krvi pri nízkych teplotách pre budúce terapeutické použitie.
Additional information URL: https://cbceva.com/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08588010018045

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

B0105UMBILICAL CORD BLOOD COLLECTION, PURIFICATION, CRYOPRESERVATION BAGS AND KITS

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

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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.