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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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PLUG FOR OMNIA GUIDED SCREW — 1 UDI-DI variant, MDD

MD Atlas
Adler Ortho S.p.A

Data from EUDAMED, last updated May 30, 2026

PLUG FOR OMNIA GUIDED SCREW

B-08052532833924

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Manufacturer: Adler Ortho S.p.A

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Device characteristics

Implantable

Legacy certificates

Certificate number: 230-01-07-DM
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: ITALCERT SRL (0426)
Validity: Nov 6, 2023

Identity & classification

Basic UDI-DI: B-08052532833924
Device name: —
Device model: PLUG FOR OMNIA GUIDED SCREW
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Version date: May 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: Adler Ortho S.p.A
SRN: IT-MF-000010164
Country: Italy
Email: info@adlerortho.com
Phone: +39 026154371

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KS4R0P44D8F60D36NN4Z4N22

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

OMNIA08052532833924