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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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Cup electrodes — 13 UDI-DI variants, MDR (FIAB S.p.A.)

MD Atlas
FIAB S.p.A.

Data from EUDAMED, last updated May 30, 2026

Cup electrodes

803300326117000003NW

13 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: FIAB S.p.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803300326117000003NW
Device name: —
Device model: Cup electrodes
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: FIAB S.p.A.
SRN: IT-MF-000005988
Country: Italy
Email: quality@fiab.it
Phone: +39 055 8497943

Variants by status

UDI-DI variants

13 UDI-DI variants

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Applied filters

basicUdiUlid01KH6J9743SCE3T19VP8H5VY98

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

F8911/LCSGR18054242447528
F8911/LCG18054242440987
F8911/SS18054242440901
F8911/LCSR18054242447498
F8911P/LCS18054242444268
F8911/LCS18054242440994
F8911/LCSR20018054953347865
F8911/LCSN18054242447481
F8911/GO18054242440918
F8911/LCSN20018054953347858
F8911/LCSG18054242447511
F8911/LCS25018054953344642
F8911/LCSV18054242447504