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Organization name
UDI-DI code
Reference / catalog number

KNEO PS TRIAL BOX S03 — Class IIa MDR by groupe lépine

MD Atlas
groupe lépine

EUDAMED last updated this device on Jul 8, 2024

KNEO PS TRIAL BOX S03

++M483L091104F9

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: groupe lépine
UDI-DI code: +M483GKAEC1030
Reference / catalog number: GKAEC103

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Manufacturer information

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

Market distribution

Primary placement in France; available across 2 countries total.

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

Device identification

Trade name: KNEO PS TRIAL BOX S03
UDI-DI code: +M483GKAEC1030
Basic UDI-DI: ++M483L091104F9
Reference / catalog number: GKAEC103
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: S03

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

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On 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.