96 results · 20ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

Esaote Endocavity ultrasonic probe, Model E 3-12, REF 120000038

FDA Enforcement
Class II ·Completed·ESAOTE S.P.A.·March 11, 2026

i.v. Station and i.v. Station ONCO Automated Drug Compounding System, Pharmacy Compounding System Device Listing Number E454448

FDA Enforcement
Class II ·Terminated·HEALTH ROBOTICS S.R.L.·January 18, 2017

SD LTM 64 PLUS, EEG Amplifier/recorder, Model/Catalog Number: SD LTM 64 PLUS, Software Version: firmware 2021.02, 2022.01 or 2022.02

FDA Enforcement
Class II ·Ongoing·Micromed S.p.A.·June 17, 2026

Ilizarov Wire Tensioner, Model 71070341, UDI (10)08033201842072(10)21HP02550(11)210831(21E434

FDA Enforcement
Class II ·Ongoing·Medicalplastic S.R.L.·November 24, 2021

TL-HEX TruLok Hexapod System, Double Row Footplates, TL-HEX Sterile, All Sizes: 120 MM, 140 MM, 160 MM, 180 MM, 200 MM. The TL-HEX TrueLock Hexapod System (TL-HEX) consists of rings, foot plates and struts to be used in conjunction with the TruLok external fixation system. The system is a metal bone fixation device for stabilization and correction during the normal healing process. The purpose of the TL-HEX System is to provide a solution for deformity correction and keeping the bone segments aligned during the healing process. The device may only be applied by a physician, who is fully responsible for the surgical and post-operative procedures of the system and is able to manage possible mechanical and software limitations. Indications for use for adults and all pediatric subgroups except newborns include: post-traumatic joint contracture which has resulted in loss of range of motion, fractures and disease which generally may result in joint contractures or loss of range of motion and fractures requiring distraction, open and closed fracture fixation, pseudoarthrosis of long bones, limb lengthening by epiphyseal or metaphyseal distraction, correction of bony or soft tissue deformities, correction of bony of soft tissue defects, joint arthrodesis, infected fractures or non unions.

FDA Enforcement
Class II ·Terminated·Orthofix Srl·June 13, 2018

ANA SCREENING

Device
EU IVDR · Eu Ivd Class B ·Dia.Metra Srl·On the market·1 country

CHORUS ANA-8

Device
EU IVDR · Eu Ivd Class B ·DIESSE Diagnostica Senese S.p.A·On the market·1 country

CHORUS ANA-8

Device
EU IVDR · Eu Ivd Class B ·DIESSE Diagnostica Senese S.p.A·On the market·1 country

Evo Autoimmune Control, ANA/ENA IgG

Device
EU IVDR · Eu Ivd Class A ·ABD SRL·On the market·2 countries

ANA Screen

Basic UDI-DI
EU IVDR · Eu Ivd Class B ·Dia.Metra Srl·1 device

Control ANA/ENA IgG - Controllo ANA/ENA IgG

Basic UDI-DI
EU IVDR · Eu Ivd Class A ·ABD SRL·1 device

Autoimmunity SPA ANA Screen - Autoimmunità SPA ANA Screen

Basic UDI-DI
EU IVDR · Eu Ivd Class A ·ABD SRL·1 device

CHORUS ANA-8

Basic UDI-DI
EU IVDR · Eu Ivd Class B ·DIESSE Diagnostica Senese S.p.A·2 devices

dIFine ANA HEp-2 Classifier

Basic UDI-DI
EU IVDR · Eu Ivd Class B ·Visia Lab S.r.l.·1 device

ALPA Medical

Authorized representative
🇮🇹 Italy·3 Manufacturers·1 Device

Donawa Lifescience Consulting Srl

Authorized representative
🇮🇹 Italy·31 Manufacturers·15 Devices

Cantel Medical (Italy) S.r.l.

Authorized representative
🇮🇹 Italy·2 Manufacturers

Ferno S.r.l.

Authorized representative
🇮🇹 Italy·4 Manufacturers

DiaSorin Italia S.p.A.

Authorized representative
🇮🇹 Italy·5 Manufacturers

Eywa srl

Authorized representative
🇮🇹 Italy·1 Manufacturer