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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 electrodes defibrillation,… — 155 UDI-DI variants, MDR

MD Atlas
FIAB S.p.A.

Data from EUDAMED, last updated May 31, 2026

Disposable electrodes defibrillation, cardioversion, cardiac stimulator, ECG

803300326808000003TV

155 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: 803300326808000003TV
Device name: —
Device model: Disposable electrodes defibrillation, cardioversion, cardiac stimulator, ECG
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Nov 25, 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

155 UDI-DI variants

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Applied filters

basicUdiUlid01KAXYEXKW6C50WXCDVC22DJTM

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

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F797008058480754427
F796708054953342894
F7750L08054953347028
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F796108033003262504
F795608033695728036
U776108054242441840
F795608054953342887
F7952W08058480757312
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F796108033695728043
F795108054953342856
F7950W08058480754458
F7950W08033695725202
F7964W08058480754502
F796508058480754236
F775308058480754281

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