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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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ASSORBENTE PER UOMO — 4 UDI-DI variants, MDR (Fater S.p.A.)

MD Atlas
Fater S.p.A.

Data from EUDAMED, last updated May 31, 2026

ASSORBENTE PER UOMO

8001480MENAU

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Fater S.p.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8001480MENAU
Device name: —
Device model: ASSORBENTE PER UOMO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: Fater S.p.A.
SRN: IT-MF-000014121
Country: Italy
Email: fater@pec-fater.it

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS090HDHMCG014M0JYR89B4F

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

800148005784508001480057845
800148005741808001480057418
800148050529208001480505292
800148050765408001480507654