33 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INTRA-LOCK INTERNATIONAL ANGLED PROSTHETIC ABUTMENTS
FDA 510(k)
FDA Class 2
·Dental
Premier
FDA UDI
PREMIER DENTAL PRODUCTS COMPANY·D6911040205·GELLHORN PESSARY #5
LOCATOR F-Tx
FDA UDI
Zest Anchors, LLC·00840481123382·LOCATOR F-Tx Abutment for Regular Crossfit (NC)...
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481123580·LOCATOR R-Tx Attachment System, Straumann Bone ...
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319700297·Turnbull Nail Nipper 4-1/2" (11.3cm), concave j...
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481128387·LOCATOR R-Tx Abutment, Straumann Bone Level, RC...
Unimed
FDA UDI
Unimed Medical Supplies, Inc.·06945664885003·ECG monitor Trunk cable/Marquette/Mindray style...
Medline
FDA UDI
MEDLINE INDUSTRIES, INC.·10884389027981·FENESTRATED DRAPE W/TAPE, 18 X 26
Specials
FDA UDI
Seaspine Orthopedics Corporation·10889981173494·Trial LTL, 13x12x05mm, Flat 7 Deg
CASTLE PERACETIC ACID BIOLOGICAL INDICATOR KIT
FDA 510(k)
FDA Class 2
·General Hospital
EMBRYON SINGLE AND DOUBLE LUMEN NEEDLES
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
PUMP IN STYLE ADVANCED BREAST PUMP GO TOTE
FDA Adverse Event
Malfunction
·MEDELA, INC.·Product code HGX·April 3, 2013
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS LLC (PR)·Product code NIQ·April 5, 2011
TUBE, GASTROINTESTINAL (AND ACCESS)
FDA Adverse Event
Injury
·C.R. BARD, INC. (BASD)·Product code KNT·May 8, 2008
ZILVER 635 SELF-EXPANDING BILIARY STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·July 3, 2017
ZILVER 635 SELF-EXPANDING BILIARY STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·January 4, 2018
ZILVER 635 BILIARY SELF-EXPANDING STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·June 1, 2018
ZILVER 635 SELF-EXPANDING BILIARY STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·May 23, 2018
ZILVER 635 SELF-EXPANDING BILIARY STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·September 12, 2017
SPINAL ANESTHESIA KIT
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC.·Product code BSP·November 6, 2018