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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

NEW WAVE LEFT TRIAL FEMUR S3 — Class IIa MDR by groupe lépine

MD Atlas
groupe lépine

EUDAMED last updated this device on Jul 5, 2024

NEW WAVE LEFT TRIAL FEMUR S3

++M483L091104F9

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: groupe lépine
UDI-DI code: +M483GNANW1430
Reference / catalog number: GNANW143

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Manufacturer information

Organization name: groupe lépine
SRN: FR-MF-000001182
Manufacturer status: Active

Related devices

1 TROCART PIN Ø2.5 L100++M483L0911YNOn the market 12/14 L TRIAL HEAD Ø32 -4++M483L091104F9On the market 12/14 L TRIAL HEAD Ø32 0++M483L091104F9On the market 130° TROCHANTERIC MARKER++M483L0909Z3On the market 133/253/H48 BOWL++M483L0999ZWOn the market

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: NEW WAVE LEFT TRIAL FEMUR S3
UDI-DI code: +M483GNANW1430
Basic UDI-DI: ++M483L091104F9
Reference / catalog number: GNANW143
Issuing entity: HIBCC

Classification

Risk category: Class IIa
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: S3

EMDN nomenclature code(s)

L091104ORTHOPAEDIC PROSTHESES POSITIONERS, 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.