10,000 results
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48ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Merlin Mount, MW HS HiR
FDA UDI
VOLK OPTICAL INC.·00811608019697·
HS Hi-R NEO 900 Microscope
FDA UDI
Haag-Streit AG·07640132987935·
HS Hi-R NEO 900 Microscope
FDA UDI
Haag-Streit AG·07640132987942·
HAAG-STREIT SURGICAL GMBH & CO. KG
FDA Adverse Event
Malfunction
·HAAG-STREIT SURGICAL GMBH &CO. KG·Product code HRM·November 6, 2020
HIR-200
FDA Adverse Event
Malfunction
·LEVEL 1, INC.·Product code KZD·November 26, 2002
HIR-202
FDA Adverse Event
LEVEL 1, INC.·Product code KZD·January 10, 2003
0IR-202
FDA Adverse Event
Malfunction
·LEVEL 1, INC.·Product code KZD·January 10, 2003
UNIPOTAR CONNECTOR
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code ---·February 7, 2005
HIR-202
FDA Adverse Event
Malfunction
·LEVEL 1, INC.·Product code KZD·January 10, 2003
HIR-200
FDA Adverse Event
Malfunction
·LEVEL 1, INC.·Product code KZD·January 10, 2003
HIR 90K
FDA Adverse Event
Injury
·ADVANCED BIONICS CORP.·Product code MCM·January 17, 2007
HIR-200
FDA Adverse Event
Injury
·LEVEL 1, INC.·Product code KZD·May 14, 2003
HIRS 90K
FDA Adverse Event
Injury
·ADVANCED BIONICS LLC·Product code MCM·April 14, 2008
Mscope Adapter Hs/Moeller Hi-R 700/1000
FDA UDI
Brainlab SE·04056481003715·
INVACARE HIR 5500
FDA Adverse Event
Injury
·INVACARE CORP·Product code FRJ·January 29, 1999
SIDEKICK
FDA Adverse Event
Malfunction
·NIPRO DIAGNOSTICS, INC·Product code NBW·February 5, 2015
Haag Streit Surgical Floor stands FS 2-11 (Ref no. 615H511) and FS 2-15 (Ref no. 615H515) in combination with the operating microscopes HS Hi-R NEO 900 (Ref no. 657 820) and HS Hi-R NEO 900A (Ref no. 657 821), with software REF 615 588 versions 2.0 to 3.3 - Product Usage: use in ophthalmology and in other disciplines with vertical direction of view
FDA Enforcement
Class II
·Ongoing·Haag-Streit USA Inc·December 30, 2020
X-PEDION
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code DQX·March 31, 2017
ONYX
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code MFE·March 31, 2017
MICROCATHETER
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code KRA·March 31, 2017