10 results
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26ms
·
Sources: EU EUDAMED, US FDA
BLADE, HANDLE, SCALPEL FORCEPS, SURGERY
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
DELTAVEN
FDA UDI
DELTA MED SPA·08032248381056·Safety I.V Catheter in PUR with closed system ,...
BD VISIDRAPE OPHTHALMIC DRAPES; BD VISIFLEX INCISE DRAPE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MAMMODIAGNOST DR
FDA 510(k)
FDA Class 2
·Radiology
GMK-REVISION FEMUR REVISION PS SIZE 6 R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·April 20, 2021
DELTAVEN Y DNL Safety I.V. Catheter in Pur with closed system: a) REF 3832572 b) REF 3842572 c) REF 3821572 d) REF 3833572 e) REF 3831572 f) REF 3810572 g) REF 3852572
FDA Enforcement
Class II
·Ongoing·Delta Med SpA·August 25, 2021
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 6, 2014
SPRINT QUATTRO SECURE
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code NVY·October 31, 2012
TRULIGN TORIC POSTERIOR CHAMBER IOL
FDA Adverse Event
Injury
·BAUSCH & LOMB INCORPORATED·Product code MJP·May 29, 2015
DELTAVEN Y DNL Safety I.V. Catheter in Pur with closed system: a) REF 3832572 b) REF 3842572 c) REF 3821572 d) REF 3833572 e) REF 3831572 f) REF 3810572 g) REF 3852572
FDA Recall
Open, Classified
·Delta Med SpA Via Guido Rossa 20 Viadana Italy·Product code FOZ·June 21, 2021