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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

TB-F 5L CR — Class III MDD by Metrimed Orvosi…

MD Atlas
Metrimed Orvosi Műszergyártó Kft.

EUDAMED last updated this device on May 19, 2026

TB-F 5L CR

B-05999539855708

On the marketClass III

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Metrimed Orvosi Műszergyártó Kft.
UDI-DI code: 05999539855708
Reference / catalog number: TB-F 5L CR

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Manufacturer information

Organization name: Metrimed Orvosi Műszergyártó Kft.
SRN: HU-MF-000004640
Manufacturer status: Active

Related devices

22HB-05999539856606On the market 22NB-05999539856590On the market 26EHB-05999539850758On the market 26EH2B-05999539858389On the market 26HB-05999539850741On 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

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Hungary; available across 2 countries total.

Country	On market since	Until
HungaryPrimary placement	Feb 16, 2012	Still on market
Bulgaria	Mar 24, 2017	Still on market

Device identification

Trade name: not provided
UDI-DI code: 05999539855708
Basic UDI-DI: B-05999539855708
Reference / catalog number: TB-F 5L CR
Issuing entity: GS1

Classification

Risk category: Class III
Applicable legislation: MDD [Directive 93/42/EEC 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: No clinical sizes registered for this device.

EMDN nomenclature code(s)

P0909030101BICOMPARTMENTAL PRIMARY IMPLANT CEMENTED FEMORAL COMPONENTS

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
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Software identification