Valve, non-rebreathing

FDA registration

Tender Corporation·1 product·🇺🇸 United States

LIV MEDICA CPR FACE MASK

FDA 510(k)

FDA Class 2 ·Anesthesiology

Valve, Non-Rebreathing

FDA classification

FDA Class 2 ·Valve, Non-Rebreathing

KMEDIC

FDA UDI

TELEFLEX INCORPORATED·24026704284287·TAYLOR SPINAL RETRACTOR 7 1/4",1 1/4"x3"

CARDINAL HEALTH

FDA UDI

Cardinal Health 200, LLC·10888439572803·KIT, OR TURNOVER

ARCHITECT PROGESTERONE CALIBRATORS (LN 7K77-01)

FDA registration

ABBOTT IRELAND DIAGNOSTICS DIVISION·1 product·🇮🇪 Ireland

Auto*Therm 395

FDA registration

METTLER ELECTRONICS CORP.·1 product·🇺🇸 United States

ARCHITECT PROGESTERONE CALIBRATORS (LN 7K77-01)

FDA registration

ABBOTT LABORATORIES·1 product·🇺🇸 United States

ARCHITECT PROGESTERONE CALIBRATORS (LN 7K77-01)

FDA registration

ABBOTT GmbH·1 product·🇩🇪 Germany

Millennium

FDA UDI

Avalign Technologies, Inc.·00190776157470·Taylor Spinal Retr 7.25" 3" Blade 1.25" Width

Millennium

FDA UDI

Avalign Technologies, Inc.·00190776097578·Taylor Spinal Retractor

CPX Tightening Tool; Cross Pin Fixation System; Tissue Protector

FDA registration

GEOTEC, INC.·1 product·🇺🇸 United States

Synergy Health AST, SRL

FDA registration

Synergy Health AST, SRL·2 products·🇨🇷 Costa Rica

MODEL 6492 UNIPOLAR TEMPORARY ATRIAL PACING LEAD

FDA 510(k)

FDA Class 2 ·Cardiovascular

AUTO*THERM 395, MODEL ME 395

FDA 510(k)

FDA Class 2 ·Physical Medicine

Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat

FDA classification

FDA Class 2 ·Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat

Electrode, Pacemaker, Temporary

FDA classification

FDA Class 2 ·Electrode, Pacemaker, Temporary