27 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IDS RAPID E PLUS SYSTEM
FDA 510(k)
FDA Class 1
·Microbiology
CoRoent
FDA UDI
Nuvasive, Inc.·00887517380739·CoRoent® Small Contoured, 10S Open
SOL-M™ Luer Lock Syringe with Exchangeable Needle
FDA UDI
Sol-Millennium Medical, Inc.·00818392010176·Used to inject medicines and vaccines into, or ...
LOCATOR®
FDA UDI
Zest Anchors, LLC·00840481100130·LOCATOR® FEMALE 10 DEGREE 10 PACK
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690192251·Apex Revision Knee Reamer – ZIMMER SHORT FLUTES...
Lingual Sheaths
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746133695·WELD LINGUAL SHEATH UNIV 030
Symmetry Diethrich
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482127810·Symmetry® Scissors, Diethrich, 25° Angle, Serra...
Shoreline ACS
FDA UDI
Seaspine Orthopedics Corporation·10889981125110·10mm, Locking Cover
MEGASYSTEM C
FDA Adverse Event
Malfunction
·WALDEMAR LINK GMBH&CO.KG·Product code KRO·July 21, 2023
e-1 etchants
FDA 510(k)
FDA Class 2
·Dental
M-SERIES PRO CPAP SYTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
Endo-Model Modular Knee Prosthesis System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575381753·Rotational Knee Joint Prosthesis,Femoral compon...
SLEEPEASY
FDA Adverse Event
Injury
·RESPIRONICS INC.·Product code BZD·April 12, 2012
REMSTAR PLUS M-SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code BZD·May 6, 2010
REMSTAR M SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code BZD·November 25, 2009
M-SERIES DC POWER SUPPLY
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·May 25, 2012
MODULAR STEM
FDA Adverse Event
Injury
·WALDEMAR LINK GMBH & CO. KG·Product code KRO·February 12, 2024
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·June 5, 2014
VITALITY 2
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 4, 2010
TRILOGY 100
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code CBK·November 14, 2012