14 results
·
20ms
·
Sources: EU EUDAMED, US FDA
VITA LAMP, MODEL 0350
FDA 510(k)
FDA Class 1
·General Hospital
ACE
FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950022502·AWL MAXILLARY #17 7-1/2" 19CM
BaseVac
FDA UDI
R. E. Morrison Equipment Inc·D13028000670·1SUR4.40+-1 | 7 User Single Surgical Vacuum + |...
ORTHO ARCH
FDA UDI
Ortho Arch Company Inc·D9098000671·BRACKET HEIGHT GAUGE - .022
ISCIENCE INTERVENTIONAL OPHTHALMIC MICROCATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ALKALINE PHOSPHATASE LIQUID REAGENT-KINETIC, MODELS A504-150 AND A504-500H
FDA 510(k)
FDA Class 2
·Clinical Chemistry
EXTENSION SET
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·May 8, 2014
ACCU-CHEK SPIRIT
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·October 17, 2012
INFUSOR SINGLEDAY 2ML/HR 12PK
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·August 16, 2010
LIFESTENT SOLO VASCULAR STENT SYSTEM
FDA Adverse Event
Malfunction
·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIP·April 13, 2020
LIFESTENT SOLO VASCULAR STENT SYSTEM
FDA Adverse Event
Injury
·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIP·February 18, 2020
LIFESTENT SOLO VASCULAR STENT SYSTEM
FDA Adverse Event
Malfunction
·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIP·April 8, 2020
LIFESTENT SOLO VASCULAR STENT SYSTEM
FDA Adverse Event
Malfunction
·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIP·April 8, 2020
Model: CT 5300; Product Code (REF): 728285; Software Versions: 5.1.0.X & 5.1.1.X;
FDA Enforcement
Class II
·Ongoing·PHILIPS MEDICAL SYSTEMS·November 5, 2025