FORCEPS 3FR CUPS REUSABLE 1DIA 220L (KS-1022CS)

FDA registration

HOYA Corporation PENTAX Lifecare Division·1 product·🇯🇵 Japan

FORCEPS 3FR CUPS REUSABLE 1DIA 220L (KS-1022CS)

FDA registration

HOYA Corporation PENTAX Lifecare Division·1 product·🇯🇵 Japan

VB-1830/VB-1530, VIDEO BRONCHOSCOPE

FDA 510(k)

FDA Class 2 ·Ear, Nose, Throat

Iris Retractor

FDA UDI

KATENA PRODUCTS, INC.·00841668103708·GRAETHER IRIS RETRACTOR W/ IRRIGATOR STR

ISOMEDIX OPERATIONS INC.

FDA registration

ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States

Isomedix Operations, Inc.

FDA registration

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

MICROPORT ORTHOPEDICS INC.

FDA registration

MICROPORT ORTHOPEDICS INC.·1 product·🇺🇸 United States

Apparatus, cautery, radiofrequency, ac-powered

FDA registration

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

ISOMEDIX OPERATIONS INC.

FDA registration

ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States

ERASER,20GA SUCTION ASPIRATION

FDA registration

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

ISOMEDIX OPERATIONS INC

FDA registration

ISOMEDIX OPERATIONS INC·1 product·🇺🇸 United States

Bronchoscope (Flexible Or Rigid)

FDA classification

FDA Class 2 ·Bronchoscope (Flexible Or Rigid)

Arthrex®

FDA UDI

ARTHREX, INC.·00888867060074·ARTHREX ECLIPSE HUMERAL HEAD, 49/20

AMBU MATIC AUTOMATIC RESUSCITATOR

FDA 510(k)

FDA Class 2 ·Anesthesiology

BIOFEEDBACK SYSTEM/3

FDA 510(k)

FDA Class 2 ·Neurology

Ventilator, Emergency, Powered (Resuscitator)

FDA classification

FDA Class 2 ·Ventilator, Emergency, Powered (Resuscitator)

Device, Biofeedback

FDA classification

FDA Class 2 ·Device, Biofeedback