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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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GUANCIALI — 9 UDI-DI variants, MDR

MD Atlas
Gruppo Industriale Formenti S.a.s.

Data from EUDAMED, last updated May 31, 2026

GUANCIALI

803264602TPGUAC5

9 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: Gruppo Industriale Formenti S.a.s.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803264602TPGUAC5
Device name: —
Device model: GUANCIALI
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Gruppo Industriale Formenti S.a.s.
SRN: IT-MF-000050869
Country: Italy
Email: marco.formenti@gruppoformenti.it
Phone: +3903626481

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01KPT3CDCTKFWM9J659QSJVPGF

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

GUDOM08032646021837
GUDUE08032646021776
GUF1108032646021806
GUF1308032646021813
GUIDM08032646021820
GUSAP08032646021851
GUSAL08032646021844
GUSIM08032646021783
GUSIL08032646021790