10 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ANTERIOR CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
FAC-4 - Class B 21 Kent - 4 Shelf Cabinet
FDA UDI
Certified Safety Manufacturing, Inc.·00766588620879·FAC-4 - Class B 21 Kent - 4 Shelf Cabinet
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471123298·K-WIRE - DOUBLE TROCAR 2.0mm DIA x 200mm
SCIg60 Infusion System
FDA 510(k)
FDA Class 2
·General Hospital
DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAM GLOVES WITH ALOE VERA, GREEN COLOR
FDA 510(k)
FDA Class 1
·General Hospital
8CH INFINITY DBS FLEX EXTN KIT, 60CM, B
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code MHY·June 3, 2024
OMNIPOD INSULIN MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code LZG·June 2, 2020
EXETER V40 STEM 44MM NO 0
FDA Adverse Event
Injury
·STRYKER IRELAND, LTD. OSTEONICS (ORTHOPAEDICS DIVI·Product code LZO·January 11, 2013
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010
6.0MM TI SIDE-OPENING SCREW 40MM
FDA Adverse Event
Injury
·SYNTHES USA·Product code NKB·July 9, 2014