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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

1061 — Class I MDR by ALFA VITA, s.r.o.

MD Atlas
ALFA VITA, s.r.o.

EUDAMED last updated this device on Mar 7, 2026

1061

859402731014GY

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ALFA VITA, s.r.o.
UDI-DI code: 08594027312557
Reference / catalog number: 1061

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Manufacturer information

Organization name: ALFA VITA, s.r.o.
SRN: CZ-MF-000051941
Manufacturer status: Active

Related devices

1065859402731004GVOn the market 1053859402731019HAOn the market 1056859402731019HAOn the market 11056859402731019HAOn the market 11054859402731002GROn the market

Market distribution

Primary placement in Czechia; available across 2 countries total.

Country	On market since	Until
CzechiaPrimary placement		Still on market
Slovakia		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08594027312557
Basic UDI-DI: 859402731014GY
Reference / catalog number: 1061
Issuing entity: GS1

Classification

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

Device details

Quantity: 3
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M050102MEDICATED PLASTERS

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

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.