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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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Neoial HC — 1 UDI-DI variant, MDD (SIFRA srl)

MD Atlas
SIFRA srl

Data from EUDAMED, last updated May 30, 2026

Neoial HC

B-08053879960007

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: SIFRA srl

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Device characteristics

ImplantableAnimal tissues / cells

Clinical investigations

Registered: No

Legacy certificates

Certificate number: 0477.MDD.21/4362
Type: refdata.legacy.mdd-certificate-type.ii-4
Notified body: Eurofins Product Testing Italy S.r.l. (0477)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-08053879960007
Device name: Neoial HC
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Version date: Sep 2, 2025

Manufacturer & authorised representative

Manufacturer

Name: SIFRA srl
SRN: IT-MF-000017908
Country: Italy
Email: silvia.baldi@sifra-srl.it
Phone: 0573 1716561

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01K45ED00VFSH9H3C1QZQ9VC97

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

N/A08053879960007