32 results
·
23ms
·
Sources: EU EUDAMED, US FDA
MODIFICATION OF: MIDMARK M-11 ULTRACLAVE STEAM STERILIZER
FDA 510(k)
FDA Class 2
·General Hospital
Eargo SE
FDA UDI
Eargo, Inc.·00850010429748·Eargo SE Plus Bundle
1505 P37,FB,2L,STANDARD,STKR
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828100236·1505 P37,FB,2L,STANDARD,STKR
MDT2 BLE Self-Monitoring Blood Glucose System
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ANTIMICROBIAL CLAVE, MODELS AG CLAVE, AG MICROCLAVE
FDA 510(k)
FDA Class 2
·General Hospital
SILKAM BLACK 3/0 (2) 75CM HR26
FDA Adverse Event
Malfunction
·B. BRAUN SURGICAL SA·Product code GAP·February 11, 2020
SER PLASTIPAK 1MLS TUB PDR1400
FDA Adverse Event
Malfunction
·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMF·July 21, 2020
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVAMEX·Product code IOR·March 5, 2013
CONCERTO CRT-D DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code NIK·February 15, 2011
PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC MILACA, INC.·Product code LWP·August 7, 2014
SILKAM BLACK 2/0 (3) 75CM HS26
FDA Adverse Event
Malfunction
·B. BRAUN SURGICAL SA·Product code GAP·February 11, 2020
SILKAM BLACK 3/0 (2) 75CM HR26
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL SA·Product code GAP·February 27, 2020
SILKAM BLACK 3/0 (2) 75CM HR26
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL SA·Product code GAP·February 20, 2020
SILKAM BLACK 3/0 (2) 75CM HR26
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL SA·Product code GAP·February 14, 2020
SILKAM BLACK 0 (3.5) 75CM HS30
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL SA·Product code GAP·January 7, 2020
SILKAM BLACK 3/0 (2) 75CM HR22
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL SA·Product code GAP·July 29, 2019
SILKAM BLACK 3/0 (2) 75CM HR22
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL SA·Product code GAP·July 29, 2019
SILKAM BLACK 3/0 (2) 45CM HS21
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL SA·Product code GAP·December 28, 2019
GORE® DUALMESH® BIOMATERIAL
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code FTL·November 12, 2020
GORE® DUALMESH® BIOMATERIAL
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code FTL·November 12, 2020