16 results
·
18ms
·
Sources: EU EUDAMED, US FDA
<GENX> DOUBLE LUMEN NEEDLE
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Inrad
FDA UDI
Inrad·00817295020640·SelectCore Variable Throw Biopsy Device 20 ga x...
SCOTT'S BENT NEEDLE TIPS (100) BLACK 20 G
FDA UDI
SCOTT'S DENTAL SUPPLY L.L.C.·D77819910201·SCOTT'S BENT NEEDLE TIPS (100) BLACK 20 G
Gen. Acces/ Instr. Tip Guard
FDA UDI
KATENA PRODUCTS, INC.·00841668112267·SURG-I-BAND ORANGE
BLUEPHASE 20I
FDA 510(k)
FDA Class 2
·Dental
G210 InviCell Plus with SignipHy pH monitoring
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
BD VACUTAINER® CTAD BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·June 4, 2018
ZMR®
FDA UDI
Zimmer, Inc.·00889024161986·
NexGen® Complete Knee Solution
FDA UDI
Zimmer, Inc.·00889024224445·
ZMR®
FDA UDI
Zimmer, Inc.·00889024161993·
BD VACUTAINER® CTAD BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 31, 2018
BD VACUTAINER® CTAD BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 3, 2018
SPINNING SPIROS CLOSED MALE LUER, RED CAP
FDA Adverse Event
Malfunction
·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·December 1, 2020
FLOGARD
FDA Adverse Event
Malfunction
·SHARP CORPORATION OSAKA JAPAN·Product code FRN·March 6, 2013
CRYSTALENS
FDA Adverse Event
Injury
·BAUSCH + LOMB·Product code NAA·February 11, 2011
SPRINT QUATTRO SECURE S
FDA Adverse Event
Malfunction
·MPRI·Product code LWS·August 8, 2014