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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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AGO DI HUBER — 1 UDI-DI variant, MDD (Multimedical s.r.l.)

MD Atlas
Multimedical s.r.l.

Data from EUDAMED, last updated May 30, 2026

AGO DI HUBER

B-08050046233698

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: Multimedical s.r.l.

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Device characteristics

Administers medicine

Legacy certificates

Certificate number: G2 014788 0026
Type: refdata.legacy.mdd-certificate-type.v
Notified body: TÜV SÜD Product Service GmbH (0123)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-08050046233698
Device name: —
Device model: AGO DI HUBER
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Multimedical s.r.l.
SRN: IT-MF-000020128
Country: Italy
Email: info@multimedical.it
Phone: +39 0375 785882

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KSJ95QCYVJ1T1TS8EXSX9GQA

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

090834/2030/M08050046233698