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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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ACCESSORI PER MAGNETOTERAPIA — 14 UDI-DI variants, MDR

MD Atlas
F&B INTERNATIONAL SRL

Data from EUDAMED, last updated May 31, 2026

ACCESSORI PER MAGNETOTERAPIA

805903793ACCMAGNETOWP

14 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: F&B INTERNATIONAL SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805903793ACCMAGNETOWP
Device name: ACCESSORI PER MAGNETOTERAPIA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 31, 2026

Manufacturer & authorised representative

Manufacturer

Name: F&B INTERNATIONAL SRL
SRN: IT-MF-000047674
Country: Italy
Email: ufftec@febinternational.com
Phone: +39 0521292516

Variants by status

UDI-DI variants

14 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KN1Q72QKFZ72BVR6CNQMS3D6

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

XXXX08059037930479
FAS005-N08059037930448
GAM00108059037930387
SGG00108059037930363
CER00108059037930349
LOM00108059037930356
GIL00108059037930394
GUA00108059037930400
MAS00108059037930370
STU002-IE08059037930455
STU003-IE08059037930462
STU00108059037930417
STU00208059037930424
STU00308059037930431