936 results · 22ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

HNI

FDA UDI
G.L.E. Gesellschaft für lichttechnische Erzeugnisse mbH·04054657500075·UV - Tanning lamp, Accession # 0631196-001 <CR>...

DISPOSABLE TWO-PART TROCAR NEEDLE

FDA Adverse Event
Malfunction ·COOK INC·Product code FBQ·December 19, 2018

STRAIGHT TROCAR SLEEVE

FDA Adverse Event
Injury ·RICHARD WOLF GERMANY (RWGMBH)·Product code FBQ·October 9, 2017

SEALING UNIT F/10/12MM TROCARS W.REDUCER

FDA Adverse Event
Injury ·AESCULAP AG·Product code FBQ·May 11, 2022

SEALING UNIT F/10/12MM TROCARS W.REDUCER

FDA Adverse Event
Injury ·AESCULAP AG·Product code FBQ·May 11, 2022

ENDOPATH TROCAR SHEATH

FDA Adverse Event
Injury ·ETHICON·Product code FBQ·February 4, 1994

ENDOPATH DISPOSABLE SURGICAL TROCAR AND SLEEVE

FDA Adverse Event
Injury ·ETHICON, INC.·Product code FBQ·January 27, 1994

KARL STORZ SPATULA AND TROCAR

FDA Adverse Event
Other ·KARL STORZ GMBH & CO.·Product code FBQ·February 25, 1994

APPLIED MEDICAL

FDA Adverse Event
Malfunction ·APPLIED·Product code FBQ·December 24, 2009

ETHICON

FDA Adverse Event
Injury ·JOHNSON & JOHNSON·Product code FBQ·June 30, 1992

ETHICON ENDOPATH

FDA Adverse Event
Other ·ETHICON, INC.·Product code FBQ·February 13, 1995

ETHICON ENDOPATH 512 X AND 512S TROCARS

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY·Product code FBQ·January 18, 1995

UNIVERSAL REDUCER 5/10/12MM 3-HOLE

FDA Adverse Event
Malfunction ·CONMED CORP.·Product code FBQ·December 5, 2005

UNIVERSAL REDUCER 5/10/12MM

FDA Adverse Event
Malfunction ·CONMED CORPORATION·Product code FBQ·October 24, 2006

COOK BRAND TRANSEPTAL NEEDLE

FDA Adverse Event
Injury ·COOK, INC.·Product code FBQ·April 16, 2019

3.2MM PELLET INSERTION TRAY #2 - STERILE / LATEX FREE

FDA Adverse Event
Injury ·75 ARKAY DRIVE·Product code FBQ·September 28, 2024

LAPAROSCOPIC TROCAR SLEEVE W/CLIP VALVE

FDA Adverse Event
Malfunction ·RICHARD WOLF GMBH·Product code FBQ·November 10, 1993

AUTO SUTURE SURGIPORT

FDA Adverse Event
Injury ·UNITED STATES SURGICAL CORPORATION·Product code FBQ·February 19, 1992

SURGIPORT 10MM

FDA Adverse Event
Injury ·UNITED STATES SURGICAL CORPORATION·Product code FBQ·February 19, 1992

LAPAROSCOPIC TROCAR SLEEVE

FDA Adverse Event
Malfunction ·R WOLF, GMBH·Product code FBQ·August 5, 1994