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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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Electrosurgery neutral electrode — 11 UDI-DI variants, MDR

MD Atlas
FIAB S.p.A.

Data from EUDAMED, last updated May 30, 2026

Electrosurgery neutral electrode

803300326106000001MN

11 UDI-DI variants

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

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

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 803300326106000001MN
Device name: —
Device model: Electrosurgery neutral electrode
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jan 16, 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

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KF2YHJ7HPX7Y7XYZRJDBZT9E

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

F7805W/V08033003264591
F7805N08033695724670
F7805NW/V08054953346588
F7805PW/V08033003264614
F7805W/6.3-508033003268353
F7905W/V08033003261194
F780508054242441949
F7805W/6.308033003264621
F7805PW/6.3-508033003268360
F780508033003260180
F7805P08054242441956