33 results · 21ms · Sources: EU EUDAMED, 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