Organization name

TRICOMED S.A.

SRN

PL-MF-000002483

Manufacturer status

Active

5 warnings recorded — scroll inside the panel to see all entries.

• Do not use if package is damaged
• Do not re-use
• Consult instructions for use
• Do not use past indicated date
• Do not resterilize

Primary placement in Poland; available across 32 countries total.

Trade name

Codubix S ŻEBRA

UDI-DI code

Primary DI

The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.

05906146508231

Basic UDI-DI

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

B-05906146508231

Reference / catalog number

MB-272-KOZE-S01

Issuing entity

UDI issuing entities

Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.

GS1

Risk category

MDR risk classes

MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.

Class IIb

Applicable legislation

MDD [Directive 93/42/EEC on medical devices]

Status

On the market

Quantity

1

Additional product description

Prosthesis for chest wall defects

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• 20 MU50
• 250 MU50

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• P900403NON-RESORBABLE FILLING AND RECONSTRUCTION DEVICES

• Class IIb medical devices in EUDAMED

No certificate specifically references this device's Basic UDI-DI.

Certificate health across this manufacturer's portfolio.