15 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NEPHELOMETER, MIC-2000 LASER
FDA 510(k)
FDA Class 1
·Clinical Chemistry
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690192978·Femoral Locating Device Bushing 3 deg
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690199250·AK3 PS Notch Reamer Guide Size 3/2+
Mini-Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR77901031·Mini Sprint Bracket McLaugh/Benn/Trev. .018" ma...
Mini-Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR77901031001·Mini Sprint Bracket McLaugh/Benn/Trev. .018" ma...
Mini-Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR77901030051·Mini Sprint Bracket McLaugh/Benn/Trev. .018" ma...
Mini-Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR77901030101·Mini Sprint Bracket McLaugh/Benn/Trev. .018" ma...
V-PRO maX 2 Low Temperature Sterilization System, V-PRO maX Low Temperature Sterilization System, V-PRO 1 Plus Low Temperature Sterilization System, V-PRO 1 Low Temperature Sterilization System
FDA 510(k)
FDA Class 2
·General Hospital
100KGY E-POLY ACETABULAR LINERS- ADDITIONAL PROFILES: +3 MAXROM AND +3 HI-WALL
FDA 510(k)
FDA Class 2
·Orthopedic
UNKNOWN LINER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·February 10, 2015
INSIGNIA
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·May 5, 2014
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 15, 2012
8F ANGIO-SEAL VASCULAR CLOSURE DEVICE VIP
FDA Adverse Event
Injury
·ST. JUDE MEDICAL·Product code MGB·August 5, 2010
BD ALARIS¿ EXTENSION SET
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·November 24, 2021
UNSPECIFIED BD INFUSION SET
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·December 22, 2022