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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

CS3-1009-16 — Class I MDR by Cardio Surgical Ltd.

MD Atlas
Cardio Surgical Ltd.

EUDAMED last updated this device on Mar 11, 2026

CS3-1009-16

539155175CS3-1009-16VV

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Cardio Surgical Ltd.
UDI-DI code: 05391551750908
Reference / catalog number: CS3-1009-16

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Manufacturer information

Organization name: Cardio Surgical Ltd.
SRN: IE-MF-000011150
Manufacturer status: Active

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CS3-1006-13 539155175CS3-1006-13V2On the market CS3-1005-23 539155175CS3-1005-23UWOn the market FSB-787-21 539155175FSB-787-213EOn the market MAH04 539155175MAH04A2On the market CS9-1048-03 539155175CS9-1048-0336On the market

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: not provided
UDI-DI code: 05391551750908
Basic UDI-DI: 539155175CS3-1009-16VV
Reference / catalog number: CS3-1009-16
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: French-Eye TC Needleholder159 mm
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

L0205NEEDLE HOLDERS, REUSABLE

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

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.