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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

2430.202 — Class IIb MDR by EUROS SAS

MD Atlas
EUROS SAS

EUDAMED last updated this device on Jun 1, 2026

2430.202

37004372V001C9

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: EUROS SAS
UDI-DI code: 03700437205999
Reference / catalog number: 2430.202

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View device family (Basic UDI)

Manufacturer information

Organization name: EUROS SAS
SRN: FR-MF-000000605
Manufacturer status: Active

Related devices

A271711137004372V001C9On the market 2430.40237004372V001C9On the market A2282041137004372V001C9On the market A2282048137004372V001C9On the market A271712137004372V001C9On 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.

Critical warnings

5 warnings recorded — scroll inside the panel to see all entries.

CW001
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW011
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in France; available across 3 countries total.

Country	On market since	Until
FrancePrimary placement		Still on market
Italy		Still on market
Portugal		Still on market

Device identification

Trade name: not provided
UDI-DI code: 03700437205999
Basic UDI-DI: 37004372V001C9
Reference / catalog number: 2430.202
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Cancellous Screw ø 6.5 mm - Length 20 mm
Additional information URL: https://eifu.euros.fr/NI.D7001B.pdf
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)03700437205999

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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.

P099003ORTHOPAEDIC PROSTHESES FIXING ELEMENTS - NOT OTHERWISE CLASSIFIED

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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