Bentley

FDA registration

PDG PRODUCT DESIGN GROUP, INC.·1 product·🇨🇦 Canada

BENTLEY MANUALLY OPERATED WHEELCHAIR

FDA 510(k)

FDA Class 1 ·Physical Medicine

artegral

FDA UDI

Merz Dental GmbH·D7091970311·anteriors; shade C2; mould UCS

Innovative7777 (SDA) - Reprocessed Steerable Introducer

FDA registration

Isomedix Operations Inc.·1 product·🇺🇸 United States

CARDIOBLATE GEMINI OUS

FDA registration

CEA Medical Manufacturing, Inc. d.b.a Nissha Medical Technologies·1 product·🇺🇸 United States

Cardioblate Gemini

FDA registration

MEDTRONIC PERFUSION SYSTEMS·1 product·🇺🇸 United States

Cardioblate® Gemini® -S Surgical Ablation Device

FDA registration

MIDWEST STERILIZATION CORP.·1 product·🇺🇸 United States

Reprocessed Steerable Introducer

FDA registration

INNOVATIVE HEALTH, LLC.·1 product·🇺🇸 United States

Cardioblate® Gemini® -S Surgical Ablation Device

FDA registration

MIDWEST STERILIZATION CORP.·1 product·🇺🇸 United States

BRAUN ExactFit™ 1 Upper arm blood pressure monitor BUA5000US

FDA registration

Helen of Troy Macao Limited·1 product·🇨🇳 China

467900 Apolipoprotein A Reagent (ApoA 2 x 100)

FDA registration

BECKMAN COULTER, INC.·2 products·🇺🇸 United States

CARDIOBLATE GEMINI SURGICAL ABLATION DEVICE, MODELS 49260 AND 49261

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Reprocessed Agilis NxT Steerable Introducer

FDA 510(k)

FDA Class 2 ·Cardiovascular

Wheelchair, Mechanical

FDA classification

FDA Class 1 ·Wheelchair, Mechanical

Reprocessed Catheter Introducer

FDA classification

FDA Class 2 ·Reprocessed Catheter Introducer

Electrosurgical, Cutting & Coagulation & Accessories

FDA classification

FDA Class 2 ·Electrosurgical, Cutting & Coagulation & Accessories