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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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SUPPOSTE GLICEROLO — 1 UDI-DI variant, MDD (New.Fa.Dem. S.r.l.)

MD Atlas
New.Fa.Dem. S.r.l.

Data from EUDAMED, last updated May 30, 2026

SUPPOSTE GLICEROLO

B-ITMF000011600R70131BY

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: New.Fa.Dem. S.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: B-ITMF000011600R70131BY
Device name: SUPPOSTE GLICEROLO
Device model: SUPPOSTE GLICEROLO
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: Mar 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: New.Fa.Dem. S.r.l.
SRN: IT-MF-000011600
Country: Italy
Email: newfadem@newfadem.it
Phone: +39 081 8195250

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KM3DYH5VFHG7QTAT8VDWDSNT

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

70131D-ITMF000011600R70131BY