Italy
Intelligence de marché des dispositifs médicaux pour Italy. Changements réglementaires, concurrents et tendances d'achats.
Signaux récents
A multicenter trial is recruiting to assess a thermosensitive hyaluronic gel for periodontal treatment efficacy.
The GREENWATER 2.0 study evaluates a urine collection device to reduce iodinated contrast agents in hospital wastewater.
This study aims to estimate long-term complication rates in ICD replacement patients over 12 months and 5 years.
GIMA SPA's XENON-AL.-3,5 V diagnostic set is registered as a Class I medical device in EUDAMED.
GIMA SPA's OTOSCOPIO F.O. SIGMA - LED is a Class I medical device registered under UDI-DI 08023279315134.
GIMA SPA's OTOSCOPIO F.O. SIGMA is a Class I medical device registered with UDI-DI 08023279315240.
GIMA SPA's OTOSCOPIO F.O. SIGMA is a Class I medical device registered with UDI-DI 08023279315257.
GIMA SPA registered the OTOSCOPIO PARKER ALOGENO OPERATIVI as a Class I medical device with UDI-DI 08023279314748.
GIMA SPA registered the Class I medical device SET DIAGNOSTICO XENON-ALOGENO - 3,5 V with UDI-DI 08023279314809.
GIMA SPA registered the BACINELLA RENIFORME, a Class I medical device, with UDI-DI 08023279266108.
TEKNOLINK 5L by Amil Care Italia S.r.l. is registered as a Class I medical device with UDI-DI 08056646471195.
GIMA SPA's OTOSCOPIO F.O. SIGMA - LED - blu is a Class I medical device registered with UDI-DI 08023279315189.
GIMA SPA registered the GIMALUX fiber optic otoscope as a Class I medical device in EUDAMED.
GIMA SPA's BACINELLA RENIFORME is a Class I medical device registered under UDI-DI 08023279266122.
GIMA SPA's BACINELLA RENIFORME INOX is a Class I medical device registered with UDI-DI 08023279265828.
GIMA SPA's BACINELLA RENIFORME INOX ECONOMICA is a Class I medical device registered under UDI-DI 08023279266429.
The Nit-Occlud® Lê VSD Spiral Coil System is evaluated for safety and effectiveness in VSD treatment across multiple countries.
BIOMERIEUX SA has registered a medical device with product code JJH in the FDA database.
ELCAM MEDICAL ITALY SPA has registered with the FDA under code 3004960482 for one medical device product.
A study compares pain perception in pediatric patients using SleeperOne vs. traditional syringe for local anesthesia.