VisuMax Laser Keratome

FDA registration

CARL ZEISS MEDITEC AG (JENA)·2 products·🇩🇪 Germany

VISUMAX LASER KERATOME

FDA 510(k)

FDA Class 2 ·Ophthalmic

Bur PM2-70 50K Diam Ø2.7

FDA UDI

Bien-Air Surgery SA·07630055502292·

Laser, Ophthalmic

FDA classification

FDA Class 2 ·Laser, Ophthalmic

DRI Oxycodone Calibrator 1000

FDA UDI

Microgenics Corporation·00884883005150·

OsteoMed

FDA UDI

OSTEOMED LLC·00845694059664·210-0253, Blue ID Tag, L 18mm RGD LT

NovaSom QSG

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

Powered light based non-laser surgical instrument with thermal effect

FDA registration

MATTIOLI ENGINEERING ITALIA SRL·1 product·🇮🇹 Italy

Chemi-SiL LB

FDA registration

B&E KOREA CO., LTD.·1 product·🇰🇷 South Korea

OsteoMed

FDA UDI

OSTEOMED LLC·00845694040921·2.0mm Left L Plate, 18mm, Rigid

Patella Drill Guide

FDA UDI

SIGNATURE ORTHOPAEDICS PTY LTD·09348215041854·

COULTER TQ-Prep Workstation

FDA registration

BECKMAN COULTER, INC.·1 product·🇺🇸 United States

cobas 8000 cobas ISE MODULE [DOUBLE]

FDA registration

ROCHE DIAGNOSTICS GMBH·78 products·🇩🇪 Germany

Analyzer

FDA registration

Diamond Diagnostics Inc.·78 products·🇭🇺 Hungary

cobas 8000 cobas ISE MODULE [DOUBLE]

FDA registration

ROCHE DIAGNOSTICS INTERNATIONAL LTD.·78 products·🇨🇭 Switzerland

Sterigenics U.S., LLC

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

ANGIO FLOW THERMODILUTION CATHETER, MODEL AF-CATH-01; ANGIOFLOW METER, MODELS HQ100 AND HQ101

FDA 510(k)

FDA Class 2 ·Cardiovascular

SILENT NIGHT V

FDA 510(k)

FDA Class 2 ·Anesthesiology

100250 component base

FDA registration

SINGLE SOURCE MEDICAL LLC·1 product·🇺🇸 United States

Catheter, Flow Directed

FDA classification

FDA Class 2 ·Catheter, Flow Directed