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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

RELEVEUR PIED GCHE 25 T2 — Class I MDR by Orliman, S.L.U.

MD Atlas
Orliman, S.L.U.

EUDAMED last updated this device on May 21, 2026

RELEVEUR PIED GCHE 25 T2

84350259ORLSM204074Q

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Orliman, S.L.U.
UDI-DI code: 08435025948525
Reference / catalog number: CP0412GA2

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Manufacturer information

Organization name: Orliman, S.L.U.
SRN: ES-MF-000001598
Manufacturer status: Active

Related devices

ANNEAU CLAVICULAIRE T1 / PÉDIATRIQUE84350259ORLSM203114AOn the market ANNEAU CLAVICULAIRE T2 / ENFANT84350259ORLSM203114AOn the market ANNEAU CLAVICULAIRE T384350259ORLSM203114AOn the market ANNEAU CLAVICULAIRE T484350259ORLSM203114AOn the market ANNEAU CLAVICULAIRE T584350259ORLSM203114AOn 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.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: RELEVEUR PIED GCHE 25 T2
UDI-DI code: 08435025948525
Basic UDI-DI: 84350259ORLSM204074Q
Reference / catalog number: CP0412GA2
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: https://www.orliman.fr/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y06120602ENERGY RETURN ANKLE-FOOT ORTHOSES

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

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Manufacturing date
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