566 results · 39ms · Sources: EU EUDAMED, US FDA

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SRI Surgical

FDA UDI
George Courey Inc·07540254001116·S L2 Surgical Gown code 7001

SRI Surgical

FDA UDI
George Courey Inc·07540254000942·Back Table Cover, 70" x 122"

SRI Surgical

FDA UDI
George Courey Inc·07540254001161·Medium, Level 2 Surgical Gown

SRI LEVEL II SURGICAL GOWN

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

SRI/SURGICAL EXPRESS SP REUSABLE SURGICAL GOWN

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

SRI SURGICAL

FDA Adverse Event
Malfunction ·SRI SURGICAL·Product code GCJ·May 14, 2010

CLOSURE TAPE USED TO SECURE VAG DELIVERY PACK

FDA Adverse Event
Other ·SRI SURGICAL·Product code FRG·August 14, 2008

VISTEC SPG 4X8 NON ST 10S 16PLY

FDA Adverse Event
Malfunction ·TYCO HEALTHCARE/ KENDALL·Product code FRO·September 15, 2006

SRI SURGICAL BREAST PACK

FDA Adverse Event
Injury ·SRI SURGICAL·Product code LRP·May 24, 2006

SRI/SURGICAL EXPRESS, INC

FDA Adverse Event
Malfunction ·SRI/SURGICAL EXPRESS, INC.·Product code FYB·January 6, 2005

STERILE PUMP PACK

FDA Adverse Event
Malfunction ·SRI SURGICAL·Product code FSM·July 2, 2011

MONOPOLAR HANDLE WITH L-HOOK

FDA Adverse Event
Malfunction ·SRI SURGICAL·Product code GEI·June 5, 2006

STERILE PACK OF TOWELS; 8 TOWEL PK (FF)

FDA Adverse Event
Malfunction ·SRI SURGICAL·Product code KKX·May 30, 2011

BURN SKIN STAPLER FROM STERILE BARCODE BURN PACK

FDA Adverse Event
Malfunction ·SRI SURGICAL·Product code FSM·July 29, 2012

SRI LIQUID PROOF SURGICAL GOWN

FDA Adverse Event
Malfunction ·SRI/SURGICAL EXPRESS, INC.·Product code FYB·February 18, 2004

STERILE STANDARD GOWN

FDA Adverse Event
Malfunction ·STERILE RECOVERIES, INC.·Product code FYA·October 21, 1997

UNK BROACH

FDA Adverse Event
Malfunction ·DEPUY IRELAND - 9616671·Product code HTQ·November 7, 2024

MICROPOWER OSCILLATOR SAW, DETACHABLE LEVER

FDA Adverse Event
Malfunction ·CONMED LINVATEC·Product code HWE·December 14, 2007

MICROPOWER OSCILLATOR SAW, DETACHABLE LEVER

FDA Adverse Event
Malfunction ·CONMED LINVATEC·Product code HWE·December 14, 2007

RAYTEC

FDA Adverse Event
Malfunction ·CARDINAL HEALTH·Product code GDY·May 8, 2013