10 results
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19ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MD TECH BIOPSY SET FOR BONE AND BONE MARROW
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Angiotech Pediatric Bone Marrow Needle. Pediatric Bone Marrow Needle. STERILE. Product Number: ION18015. 510k K980196. MEDICAL DEVICE TECHNOLOGIES, INC. 3600 Southwest 74th Avenue, Gainesville, Florida 32608 U.S.A. Intended Use: Pediatric Bone Marrow Needle
FDA Recall
Terminated
·Medical Device Technologies, Inc.·Product code KNW·September 1, 2009
DeltaForm HD
FDA UDI
Merz Dental GmbH·D7091980196·DeltaForm HD upper posteriors, S, BL4 -MADE IN ...
ENDOPATH ENDOSCOPIC MULTIFEED STAPLER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code GAG·January 14, 1998
On Call Express Mobile Blood Glucose Monitoring System
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Z3D CONTRAST ACUITY
FDA 510(k)
FDA Class 2
·Radiology
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 27, 2013
JOHNSON & JOHNSON COMPANY
FDA Adverse Event
Injury
·Product code JWH·February 4, 2011
TRILOGY 100
FDA Adverse Event
Malfunction
·RESPIRONICS INC.,·Product code CBK·July 2, 2014
1.85MM TI MATRIX SCREW SELF-TAPPING/4MM
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code JEY·January 21, 2015