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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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FlexiOss — 1 UDI-DI variant, MDD (Medical Inventi S.A.)

MD Atlas
Medical Inventi S.A.

Data from EUDAMED, last updated May 30, 2026

FlexiOss

B-05903728887012

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: Medical Inventi S.A.

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Device characteristics

Implantable

Clinical investigations

Registered: No

Legacy certificates

Certificate number: 1434-MDD-269/2021
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-05903728887012
Device name: FlexiOss
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: Jan 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Medical Inventi S.A.
SRN: PL-MF-000007157
Country: Poland
Email: biuro@medicalinventi.pl

Variants by status

UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01GVDM38ZKA83KEN5ZGXRQ0FHY

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

Bone replacement composite FlexiOss®05903728887012