24 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Non-Sterile, Powder Free Nitrile Examination Gloves, Tested for use with Chemotherapy Drugs (Blue, Cobalt Blue)
FDA 510(k)
FDA Class 1
·General Hospital
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·14026704912305·
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704292510·
NA
FDA UDI
KEY SURGICAL, INC.·10849771048876·K-Wires, Double trocar, .054-inch (1.4mm) diame...
K-Wire w. double end trocarpoint 1.40mm/102mm, 6 pcs./unit
FDA UDI
mahe medical gmbh·EMAHKM711040·K-Wire w. double end trocarpoint
1.40mm...
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659484054·K-Wire w. double end trocarpoint _x000D_...
Tasso+ Convenience Kit
FDA UDI
Tasso Inc.·00860006434533·Tasso+ allows self-collection of a capillary bl...
UHEAD
FDA UDI
Stryker GmbH·00886385013688·Stem Trial; Std. Collar; Size 1
GUTTA PERCHA POINTS
FDA UDI
DiaDent Group International·08806383543859·Gutta Percha Points is used to root canal filin...
VACUTRON
FDA UDI
Allied Medical, LLC·00026072009529·
ACUTE PORTABLE EXCHANGE DEIONIZATION (PEDI) SYSTEM, CENTRAL PEDI SYSTEM, BACK-UP PEDI SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
REMIN PRO
FDA 510(k)
FDA Class 1
·Dental
VACUTRON
FDA UDI
Allied Medical, LLC·00026072009550·
VACUTRON
FDA UDI
Allied Medical, LLC·00026072009567·
VACUTRON
FDA UDI
Allied Medical, LLC·00026072009543·
VACUTRON
FDA UDI
Allied Medical, LLC·00026072009536·
VACUTRON
FDA UDI
Allied Medical, LLC·00026072009574·
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2016
COBAS E-ELECSYS ANTI HCV ELECSYS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code MZO·August 23, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·July 11, 2011