25 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
hCG Urine Test Strip, hCG Urine Test Cassette, hCG Urine Test Midstream
FDA 510(k)
FDA Class 2
·Clinical Chemistry
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772777655·LUMBAMED BASIC DORSAL STAYS M SILVER III
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780182122·Integra® Jarit® Little Retractor, 7-1/2", 11.6m...
7000 CONNECTORS
FDA UDI
HANS RUDOLPH, INC.·00817136022192·CONN 28.6IDORG X28.6IDORG 7000
GERALD TISSUE FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896060159·GERALD TISSUE FORCEPS CROSS SERRATED TIP
Initia Total Hip System
FDA UDI
KYOCERA MEDICAL CORPORATION·04580810058027·"STDHO LINER 32-46
Size:32-46
Type:Flat, HO
32m...
DESS dental smart solutions
FDA UDI
TERRATS MEDICAL SL.·08435457202950·External Hex Universal
Initia Total Hip System
FDA UDI
KYOCERA CORPORATION·04547898307263·STDHO LINER 32-46
Minuteman
FDA UDI
Spinal Simplicity, LLC·M9432001330000·Cobb Spinal Elevator 28cm
MENICON Z
FDA 510(k)
FDA Class 2
·Ophthalmic
MODIFICATION TO THE MAESTRO SYSTEM
FDA 510(k)
FDA Class 2
·Dental
BONE SCREW 6,5 H.30MM
FDA Adverse Event
Injury
·LIMA CORPORATE S.P.A.·Product code LPH·February 7, 2020
HNM MEDICAL
FDA UDI
HNM STAINLESS, LLC.·00842962160305·MINI CASE, 7"X3"X1", W/SILICONE MAT
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·October 15, 2008
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 10, 2011
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 1, 2013
ENDEAVOR RX
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIQ·August 19, 2021
RESOLUTE INTEGRITY RX
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIQ·August 19, 2021
CURRENT HEALTH MONITORING SYSTEM GEN 2 (G2)
FDA Adverse Event
Death
·CURRENT HEALTH LTD·Product code MSX·September 9, 2024
ANSPACH***REF SP-4605-00***Arthroscopic Suture Anchor assembly with Suture Threader***Rx Only*** This device is intended to be used with Anspach Systems
FDA Enforcement
Class II
·Terminated·The Anspach Effort, Inc.·July 2, 2014