22 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NUMED COEFFICIENT PTV CATHETERS
FDA 510(k)
FDA Class 2
·Cardiovascular
CoverLoc™ Volar Plate
FDA UDI
TORNIER, INC.·00846832001446·FULLY THREADED SCREW
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00141241·
NA
FDA UDI
Stryker GmbH·04546540246677·DRILL, WL 27MM, STRYKER-SHAFT
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033564042·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033563991·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033564011·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033564059·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033564028·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033564004·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033564035·
LIFEPORT VASCULAR ACCESS SYSTEM
FDA Adverse Event
Injury
·STRATO/INFUSAID INC.·Product code LJT·September 23, 1998
IL TEST PROS
FDA 510(k)
FDA Class 2
·Hematology
ARTHREX UNIVERS 30 SHOULDER PROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
VACUETTE BLOOD COLLECTION TUBE 3ML K2E K2EDTA
FDA Adverse Event
Malfunction
·GREINER BIO-ONE NA INC.·Product code JKA·November 2, 2020
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·January 23, 2018
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 21, 2013
QUICKFLEX MICRO LV LEAD
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·March 10, 2011
ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Injury
·STAAR SURGICAL CO.·Product code HQL·March 13, 2008
Aqauapak 728 SW, 760 ML W/028 Adaptor, Intl, Product No. 403728; Aqauapak 1028 SW, 1070 ML/W028 Adaptor, Intl, Product No. 404128; Aqauapak 428 SW, 440 ML W/028 Adaptor, Intl, Product No. 404428; Aquapak 728 SW, 760 ML W/028 Adaptor, Product No. 037-28; Aquapak SW/EAU Sterile, 760 ML W/Adaptor, Product No. 037-28C; Aquapak 728 SW, 760 ML W/28 Adaptor, French, Product No. 037-02F; Aquapak 733 SW, 760 ML W/033 Adaptor, Product No. 037-33; Aquapak 735 HNS, 760 ML W/028 Adaptor, Product No. 037-35; Aquapak 739 FNS, 760 ML W/028 Adaptor, Product No. 037-39; Aquapak 0.9% NACL, 760 ML W/Adaptor, Product No. 037-39C; Aquapak 770 HNS, 760 ML W/033 Adaptor, Product No. 037-70; Aquapak 1028 SW, 1070 ML W/028 Adaptor, Product No. 041-28; Aquapak SW/EAU Sterile, 1070 ML W/Adaptor, Product No. 041-28C; Aquapak 1033 SW, 1070 ML W/033 Adaptor; Product No. 041-33; Aquapak 1035 HNS, 1070 ML W/028 Adaptor, Product Code 041-35; Aquapak 428 SW, 440 ML W/028 Adaptor, Product No. 044-28; Aquapak SW/EAU Sterile, 440 MLW/Adaptor, Product No. 044-28C; Aquapak 428 SW, 440 ML W/028 Adaptor, French, Product No. 044-28F; Aquapak 433 SW, 440 ML W/033 Adaptor, Product No. 044-33; Aquapak 435 HNS, 440 ML W/028 Adaptor, Product No. 044-35; Aquapak 470 HNS, 440 ML W/033 Adaptor, Product No. 044-70. Used in anesthesiology.
FDA Enforcement
Class II
·Terminated·Teleflex Medical·December 10, 2014