30 results
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20ms
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Sources: EU EUDAMED, US FDA
POWDER FREE LATEX EXAMINATION GLOVES WITH WATER EXTRACTABLE PROTEIN LABELING CLAIM. (50 MICROGRAMS OR LESS)
FDA 510(k)
FDA Class 1
·General Hospital
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00271011·
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00270211·
LOCATOR, Dentsply Sirona System
FDA UDI
Zest Anchors, LLC·00840481131806·LOCATOR R-Tx Limited Range Retention Inserts, L...
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481126048·LOCATOR R-Tx Limited Range Retention Inserts, L...
JOBST Custom Seamless Soft
FDA UDI
BSN-Jobst GmbH·04059993124275·CUSTOM SEAMLESS SOFT 1/PANTY/CLOSED TOE/FULL CO...
JOBST Custom Seamless Soft
FDA UDI
BSN-Jobst GmbH·04059993133352·CUSTOM SEAMLESS SOFT 1/THIGH HIGH/CLOSED TOE/FR...
JOBST Custom Seamless Soft
FDA UDI
BSN-Jobst GmbH·04059993129812·CUSTOM SEAMLESS SOFT 1/MID THIGH HIGH/CLOSED TO...
JOBST Custom Seamless Soft
FDA UDI
BSN-Jobst GmbH·04059993143283·CUSTOM SEAMLESS SOFT 2/CHAP STYLE/CLOSED TOE/FU...
JOBST Custom Seamless Soft
FDA UDI
BSN-Jobst GmbH·04059993125739·CUSTOM SEAMLESS SOFT 1/CHAP STYLE/CLOSED TOE/FU...
JOBST Custom Seamless Soft
FDA UDI
BSN-Jobst GmbH·04059993131334·CUSTOM SEAMLESS SOFT 1/AG-HT ONE LEG PANTY/CLOS...
HUMAN IGG SUBCLASS KIT USE WITH THE BECKMAN IMAGE ANALYZER
FDA 510(k)
FDA Class 2
·Immunology
BREEZE SLEEPGEAR WITH DREAMSEAL
FDA 510(k)
FDA Class 2
·Anesthesiology
NI
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code LHI·May 13, 2022
VENTED MICRO VOL.INLET, N/S
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code LHI·March 28, 2022
VALVE SET, EM2400
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code LHI·April 7, 2022
VALVE SET, EM2400
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code LHI·August 8, 2022
TOTALCARE DUO BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·February 13, 2013
LCS COMPLETE FEM POR R STD+
FDA Adverse Event
Injury
·DEPUY-CORK, A DIVISION OF DEPUY ORTHOPAEDICS·Product code MBH·February 17, 2011
GE OEC 8800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS, INC·Product code JAA·February 26, 2008