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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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Ring electrode — 5 UDI-DI variants, MDR (FIAB S.p.A.)

MD Atlas
FIAB S.p.A.

Data from EUDAMED, last updated May 31, 2026

Ring electrode

803300326117000012NX

5 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: 803300326117000012NX
Device name: —
Device model: Ring electrode
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 13, 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

5 UDI-DI variants

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Applied filters

basicUdiUlid01KHBEC4XZ1DZGN94ZEFRJD31F

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

F8903/408054242441628
F8903/508054242444513
F8903/108054242441598
F8903/308054242441611
F8903/208054242441604