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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

KC4718 — Class I MDR by Cair LGL

MD Atlas
Cair LGL

EUDAMED last updated this device on Mar 25, 2026

KC4718

3661657ASP01UP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Cair LGL
UDI-DI code: 13661657004137
Reference / catalog number: KC4718

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Manufacturer information

Organization name: Cair LGL
SRN: FR-MF-000007921
Manufacturer status: Active

Related devices

NCB51373661657ENT02VNOn the market NCB51173661657ENT02VNOn the market NCB41173661657ENT02VNOn the market TB300U3661657ENT02VNOn the market NCB51273661657ENT02VNOn 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 France; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 13661657004137
Basic UDI-DI: 3661657ASP01UP
Reference / catalog number: KC4718
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A0380TUBULAR DEVICES - ACCESSORIES

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
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Software identification