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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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Disposable sterile electrocautery — 11 UDI-DI variants, MDR

MD Atlas
FIAB S.p.A.

Data from EUDAMED, last updated May 31, 2026

Disposable sterile electrocautery

803300326007000003ML

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: 803300326007000003ML
Device name: —
Device model: Disposable sterile electrocautery
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Sep 18, 2025

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

basicUdiUlid01K5DNR1HPKCC1MWGN88GTZK9W

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

F727708058480754779
F7234/118033695726954
F7244/128058480756418
F7288/128058480756425
F725508058480754755
F7255/108054751932365
F726608058480754731
F728808058480754748
F7255UF08058480756377
F724408058480753536
F723408058480754762