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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

CS0360 — IVDR Class A IVDR by SC SPD STAR SRL

MD Atlas
SC SPD STAR SRL

EUDAMED last updated this device on May 15, 2026

CS0360

5944751IVDRC67

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: SC SPD STAR SRL
UDI-DI code: 05944751001488
Reference / catalog number: CS0360

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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: 05944751001488
Basic UDI-DI: 5944751IVDRC67
Reference / catalog number: CS0360
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic 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.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05944751001488

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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.

W05019001FAECES COLLECTION DEVICES

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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