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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

VS-103/2 — Class I MDR by VAKUFORM s.r.o.

MD Atlas
VAKUFORM s.r.o.

EUDAMED last updated this device on May 6, 2026

VS-103/2

859422551VAKUFORMHR

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: VAKUFORM s.r.o.
UDI-DI code: 08594225510069
Reference / catalog number: VS-103/2

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Manufacturer information

Organization name: VAKUFORM s.r.o.
SRN: CZ-MF-000044602
Manufacturer status: Active

Related devices

VS-117859422551VAKUFORMHROn the market VS-105859422551VAKUFORMHROn the market VS-104859422551VAKUFORMHROn the market VS-109859422551VAKUFORMHROn the market VS-108859422551VAKUFORMHROn 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.

Market distribution

Primary placement in Czechia; available across 1 country total.

Country	On market since	Until
CzechiaPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08594225510069
Basic UDI-DI: 859422551VAKUFORMHR
Reference / catalog number: VS-103/2
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: Vakuová dlaha horní končetiny je mnohonásobně použitelný fixační prostředek pro poskytnutí přednemocniční neodkladné péče. Je určena k šetrné stabilizaci a transportní imobilizaci horní končetiny.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M03050299BANDAGES AND SPLINTS - OTHER

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

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Manufacturing date
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