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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

Adapter with screws-adjustable — Class I MDR

MD Atlas
SC ELITEX PROTHETIC SRL

EUDAMED last updated this device on Jul 5, 2024

Adapter with screws-adjustable

5949096398ELPROBWZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SC ELITEX PROTHETIC SRL
UDI-DI code: 05949096398125
Reference / catalog number: OB33

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View device family (Basic UDI)

Manufacturer information

Organization name: SC ELITEX PROTHETIC SRL
SRN: RO-MF-000042662
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Romania; available across 1 country total.

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

Device identification

Trade name: Adapter with screws-adjustable
UDI-DI code: 05949096398125
Basic UDI-DI: 5949096398ELPROBWZ
Reference / catalog number: OB33
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: Adaptoarele cu suruburi-mobile de laminare OB33 se montează prin laminare într-o cupă de proteză. Ele folosesc ca elemente de racord între cupa protetică şi componentele protetice distale / articulatiile de genunchi protetice (ex. OB40,OB41,OB45,OB46/OB50,OB51C,OB52, ....)
Additional information URL: https://www.orthobar.ro/
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)05949096398125

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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.

Y062415TRANSFEMORAL PROSTHESES (FOR AMPUTATION ABOVE KNEE)

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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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.