41 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IMMULITE 2000 DIGOXIN, MODELS L2KDI2 (200 TESTS) AND L2KDI6 (600 TESTS)
FDA 510(k)
FDA Class 2
·Clinical Toxicology
ICU Medical
FDA UDI
ICU MEDICAL, INC.·00840619023324·5" Bag Spike Adapter w/Spiros™, Vented Cap
Aztec
FDA UDI
Aztecmed/Ent LLC·B87110123010·Buck Ear Curette size 1 Sharp/angled
JOBST Custom Seamless Soft
FDA UDI
BSN-Jobst GmbH·04059993139507·CUSTOM SEAMLESS SOFT 2/AG-HT ONE LEG PANTY/CLOS...
JOBST Custom Seamless Soft
FDA UDI
BSN-Jobst GmbH·04059993137312·CUSTOM SEAMLESS SOFT 3/AG-HT ONE LEG PANTY/CLOS...
JOBST Custom Seamless Soft
FDA UDI
BSN-Jobst GmbH·04059993131792·CUSTOM SEAMLESS SOFT 1/AG-HT ONE LEG PANTY/CLOS...
NESS L300-Plus System
FDA UDI
BIONESS INC.·07290110483012·L300 Plus US System Kit, Right (regular)
5" BAG SPIKE ADAPTOR W/ SPIROS
FDA Adverse Event
Malfunction
·ICU MEDICAL, INC.·Product code FPA·September 19, 2014
IMMUNOWELL EA (D) IGG TEST
FDA 510(k)
FDA Class 1
·Microbiology
SUPER 12
FDA 510(k)
FDA Class 2
·Dental
ALARIS PUMP MODULE ADMINISTRATION SET
FDA Adverse Event
Malfunction
·CAREFUSION CORPORATION·Product code FPA·July 24, 2013
DEPTH DEV,2.7/3.5 /4.0MMLO-PRO
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HTJ·February 20, 2024
DEPTH DEV,2.7/3.5 /4.0MMLO-PRO
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HTJ·March 18, 2024
UNK NEXGEN CT-FLEX FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·March 12, 2013
ACCU-CHEK FLEXLINK PLUS
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code FRN·March 4, 2011
PATHFINDER
FDA Adverse Event
Malfunction
·ABBOTT SPINE·Product code HXX·March 12, 2008
PREMICRON GREEN 4/0(1,5)4X45 HR13 TOM
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL SA·Product code GAT·January 29, 2020
INDIGO SYSTEM LIGHTNING 12
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code QEW·June 3, 2021
PREMICRON GREEN 2/0 (3) 75CM HR26 (M)
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL SA·Product code GAW·June 28, 2019
PREMICRON GREEN 2/0 (3) 30CM SKR19(M)
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL SA·Product code GAT·February 3, 2020