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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

Sterile Non-Woven Euroswabs — Class I MDR by GS Medical

MD Atlas
GS Medical

EUDAMED last updated this device on Jul 31, 2024

Sterile Non-Woven Euroswabs

539151646GSMNSNWW2

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: GS Medical
UDI-DI code: 05391516467018
Reference / catalog number: 20018

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Manufacturer information

Organization name: GS Medical
SRN: IE-MF-000010064
Manufacturer status: Active

Market distribution

Primary placement in Ireland; available across 1 country total.

Placed on the market in Ireland; per-country availability dates not published.

Device identification

Trade name: Sterile Non-Woven Euroswabs
UDI-DI code: 05391516467018
Basic UDI-DI: 539151646GSMNSNWW2
Reference / catalog number: 20018
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: 5
Additional product description: 30g/m3 5cm X 5cm 8ply Sterile
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 5 MU10

EMDN nomenclature code(s)

M0202010101NON-WOVEN FOLDED GAUZES, WITHOUT X-RAY DETECTABLE THREAD, STERILE

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

Drain Swabs539151646GSMNSNWW2On the market Euroswabs539151646GSMSGSKSOn the market Non Sterile Absorbent Pads539151646GSMNSWPWFOn the market Non Sterile Absorbent Pads539151646GSMNSWPWFOn the market Non Sterile Absorbent Pads539151646GSMNSWPWFOn 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.