Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

P 26-48 — Class III MDD by Metrimed Orvosi…

MD Atlas
Metrimed Orvosi Műszergyártó Kft.

EUDAMED last updated this device on May 20, 2026

P 26-48

B-05999539851717

On the marketClass III

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Metrimed Orvosi Műszergyártó Kft.
UDI-DI code: 05999539851717
Reference / catalog number: P 26-48

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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 1 country total.

Country	On market since	Until
HungaryPrimary placement	May 1, 2004	Still on market

Device identification

Trade name: not provided
UDI-DI code: 05999539851717
Basic UDI-DI: B-05999539851717
Reference / catalog number: P 26-48
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)

P090803010199PRIMARY IMPLANT CEMENTED ACETABULAR CUPS - OTHER

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