14 results
·
18ms
·
Sources: EU EUDAMED, US FDA
IMX TOTAL B-HCG
FDA 510(k)
FDA Class 2
·Clinical Chemistry
REVELATION DIAMOND
FDA UDI
Ss White Burs, Inc.·D6909125352·REVELATION DIAMOND 850-014F - 5 PACK
Gen. Acces/ Instr. Tip Guard
FDA UDI
KATENA PRODUCTS, INC.·00841668110898·TIP GUARDS VENTED YELLOW PACK OF 100
Gen. Acces/ Instr. Tip Guard
FDA UDI
KATENA PRODUCTS, INC.·00841668110874·TIP GUARDS VENTED GREEN PACK OF 100
Unity
FDA UDI
DIOMEDICAL CO.,LTD.·08800113960282·Unity Sacroiliac Joint Fixation - Threaded Coun...
HNM MEDICAL
FDA UDI
HNM STAINLESS, LLC.·00842962159286·BLUNT OBTURATOR FOR 3.4MM OPERATING SHEATH 0° T...
GENESIS REUSABLE RIGID CONTAINER SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
DRG DISPOSABLE VAGINAL SPECULUM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
HEARTSTART ONSITE
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 14, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 13, 2013
COLLEAGUE CX VOLUMETRIC INFUSION PUMP SINGLE CHANNEL
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·December 2, 2010
DATASCOPE MR MONITOR
FDA Adverse Event
Malfunction
·DATASCOPE CORP./PT MONITORING DIVISION·Product code MHX·January 23, 2003
PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code HSX·October 15, 2025
GENESIS UNI KNEE FEMORAL COMPONENT COCR
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code HSX·May 23, 2025