AGC V2 REVISION KNEE SYSTEM

FDA registration

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

Synergy Health Sterilisation UK Ltd

FDA registration

Synergy Health Sterilisation UK Ltd·1 product·🇬🇧 United Kingdom

AGC V2 REVISION KNEE SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

Polystar HK

FDA UDI

Merz Dental GmbH·D7091984054·anteriors; shade A2; mould R 60

Exeter Hip System

FDA registration

HOWMEDICA OSTEONICS CORP·1 product·🇺🇸 United States

Stryker Injectable Cement

FDA registration

Nelipak Healthcare Packaging·1 product·🇮🇪 Ireland

ASP Cidex Plus Solution Test Strips

FDA registration

ALBERT BROWNE LTD.·1 product·🇬🇧 United Kingdom

ASP CIDEX Plus Solution Test Strips

FDA registration

ADVANCED STERILIZATION PRODUCTS·1 product·🇺🇸 United States

Synergy Health Westport Ltd

FDA registration

Synergy Health Westport Ltd·1 product·🇮🇪 Ireland

Exeter Hip System

FDA registration

HOWMEDICA INTERNATIONAL S. DE R.L.,·1 product·🇮🇪 Ireland

Exeter Hip System

FDA registration

STRYKER IRELAND OSTEONICS·1 product·🇮🇪 Ireland

BT2000 Automated Manifold Kit

FDA registration

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

5.0 MHZ ARRAY INTRAVAGINAL TRANSDUCER

FDA 510(k)

FDA Class 2 ·Radiology

MODIFICATION OF THE CEDIA DIGOXIN ASSAY

FDA 510(k)

FDA Class 2 ·Clinical Toxicology

Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

FDA classification

FDA Class 2 ·Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Enzyme Immunoassay, Digoxin

FDA classification

FDA Class 2 ·Enzyme Immunoassay, Digoxin

System, Imaging, Pulsed Doppler, Ultrasonic

FDA classification

FDA Class 2 ·System, Imaging, Pulsed Doppler, Ultrasonic