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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

VO100 — Class I MDR by SC SPD STAR SRL

MD Atlas
SC SPD STAR SRL

EUDAMED last updated this device on May 6, 2026

VO100

5944751VATAAJ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SC SPD STAR SRL
UDI-DI code: 05944751000320
Reference / catalog number: VO100

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View device family (Basic UDI)

Manufacturer information

Organization name: SC SPD STAR SRL
SRN: RO-MF-000004404
Manufacturer status: Active

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Certificates

Certificate health across this manufacturer's portfolio.

MDR.2292-2025/0006Issued
Quality assuranceNotified body: 2292Expiry: Apr 14, 2030

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Romania; available across 1 country total.

Country	On market since	Until
RomaniaPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05944751000320
Basic UDI-DI: 5944751VATAAJ
Reference / catalog number: VO100
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: Descriere: Produs fabricat din fibre de bumbac albit, asigură absorbție ridicată și protecție optimă. Utilizare: În practica medicală, chirurgicală și îngrijire personală, uz extern. Instrucțiuni speciale: Nu se aplică pe rănile adânci. Nu se lasă la îndemâna și la vederea copiilor. Depozitare: În încăperi uscate, curate, ferite de lumina directă a soarelui.
Additional information URL: No additional information URL provided by the manufacturer.
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)05944751000320

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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.

M010101HYDROPHILIC COTTON

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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