VERIFY Bowie Dick Test Card (S3095) (HP-MF)

FDA registration

STERIS Corporation·1 product·🇺🇸 United States

BOWIE-DICK TEST CARD CATALOG NUMBER 008018

FDA 510(k)

FDA Class 2 ·General Hospital

Precept

FDA UDI

Nuvasive, Inc.·00887517387981·PRECEPT Screw Shank, 7.0x45mm Modular

Lactophenol Aniline Blue

FDA registration

CalibreScientific US, Inc.·1 product·🇺🇸 United States

Miya Hook

FDA registration

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

MEGA PLUS MIS SPINE SYSTEM

FDA UDI

BK MEDITECH CO.,LTD.·08809916497353·Long-arm Multi-Axial Fenestrated Screw, Ø7.0 x ...

Indicator, Physical/Chemical Sterilization Process

FDA classification

FDA Class 2 ·Indicator, Physical/Chemical Sterilization Process

Arthrex®

FDA UDI

ARTHREX, INC.·00888867133891·DRILL BIT, 4.5MM

Blom-Singer Laryngectomy Tubes

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

MODEL 6208,6209,6210,6211,6212,6214 (PLI'S)

FDA 510(k)

FDA Class 3 ·Cardiovascular

SC-1000 WITH SUFFIXES (SCAN CONVERTER)

FDA 510(k)

FDA Class 2 ·Radiology

System, X-Ray, Fluoroscopic, Image-Intensified

FDA classification

FDA Class 2 ·System, X-Ray, Fluoroscopic, Image-Intensified

Permanent Pacemaker Electrode

FDA classification

FDA Class 3 ·Permanent Pacemaker Electrode