32 results · 23ms · Sources: EU EUDAMED, US FDA

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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