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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

1057 — 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

1057

859402731016H4

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ALFA VITA, s.r.o.
UDI-DI code: 08594027313844
Reference / catalog number: 1057

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Manufacturer information

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

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: 08594027313844
Basic UDI-DI: 859402731016H4
Reference / catalog number: 1057
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: 1
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)

M050201EXTENSIBLE NON-WOVEN 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

Related devices

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