Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

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.

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

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

F7965/NG08054751930187
F7952/20008054953340401
F7965W/NG08054751930279
F797108058480754434
F7956W08054242440065
F797008033003262856
U796108054242441796
F7953W08054242446692
F795508033003260524
F775208033003268483
F7955W08058480757329
F7967W08054751932280
F775508033003268513
F775908033003268537
F795208058480754137
F7956W08058480754496
F765208058480757541
F796208033003262634
F795508033695728029
F7960W08054751930231
F795208033695727992
F795808054953343167
F765008058480757527
F797208058480754441
F7952W08058480754472

1 2 3 4 5