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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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ZOOM TERMINAL 8mm-25mm — 8 UDI-DI variants, MDR (FISIOLINE SRL)

MD Atlas
FISIOLINE SRL

Data from EUDAMED, last updated May 31, 2026

ZOOM TERMINAL 8mm-25mm

805794917009ACLT3U

8 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: FISIOLINE SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805794917009ACLT3U
Device name: —
Device model: ZOOM TERMINAL 8mm-25mm
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: FISIOLINE SRL
SRN: IT-MF-000027924
Country: Italy
Email: fisioline@fisioline.com
Phone: 0172470432

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01KS049KFVK5QHE1QY1VGDEX94

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

TERMBECCMANLAS08057949171379
TERMOTTCHIRU08057949171430
MANTERAPEUTICO08057949171942
TERMPORTALENTE908057949171669
TERMPOLENLUMIXQ08057949171812
TERMINALESFERA08057949171676
TERMZOOMMANLAS08057949171331
TERMZOOMQ08057949171805