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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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Codubix S ŻEBRA — 1 UDI-DI variant, MDD (TRICOMED S.A.)

MD Atlas
TRICOMED S.A.

Data from EUDAMED, last updated May 30, 2026

Codubix S ŻEBRA

B-05906146508354

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: TRICOMED S.A.

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Device characteristics

Implantable

Legacy certificates

Certificate number: 1434-MDD-164/2020
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A. (1434)
Validity: May 27, 2024

Identity & classification

Basic UDI-DI: B-05906146508354
Device name: Codubix S ŻEBRA
Device model: RZ7
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: Apr 3, 2026

Manufacturer & authorised representative

Manufacturer

Name: TRICOMED S.A.
SRN: PL-MF-000002483
Country: Poland
Email: sekretariat@tricomed.com
Phone: +48 42 689 65 20

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KN931D7XQNFV5RMV83E8H6JA

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

MB-272-KOZE-S0705906146508354