EVIS EXERA II ULTRASONIC BRONCHOFIBERVIDEOSCOPE

FDA UDI

OLYMPUS MEDICAL SYSTEMS CORP.·04953170341830·

ULTRASOUND BRONCHOSCOPE

FDA UDI

PENTAX OF AMERICA, INC.·04961333232208·LINEAR ULTRASOUND VIDEOBRONCHOSCOPE 2.0C (REFUR...

PENTAX

FDA UDI

HOYA CORPORATION·04961333227112·Perform cleaning, high-level disinfection, and/...

PENTAX Medical

FDA UDI

HOYA CORPORATION·04961333232130·PENTAX Medical Round-Trip Carrying Case VE-B24

FUJIFILM

FDA UDI

FUJIFILM CORPORATION·04547410104349·This product is intended to inject the reproces...

FUJIFILM

FDA UDI

FUJIFILM CORPORATION·04547410330182·The Fujinon/Fujifilm Ultrasonic Endoscope EB-53...

EVIS EXERA II ULTRASONIC BRONCHOFIBERVIDEOSCOPE

FDA UDI

OLYMPUS MEDICAL SYSTEMS CORP.·04953170243226·

EVIS EXERA II ULTRASONIC BRONCHOFIBERVIDEOSCOPE

FDA UDI

OLYMPUS MEDICAL SYSTEMS CORP.·04953170356360·BF-UC180F ULTRASOUND BRONCHOSCOPE

FUJIFILM

FDA UDI

FUJIFILM CORPORATION·04547410111392·This product is intended to prevent backflow of...

EVIS EXERA II ULTRASONIC BRONCHOFIBERVIDEOSCOPE

FDA UDI

OLYMPUS MEDICAL SYSTEMS CORP.·04953170356353·

EVES EUS ULTRASOUND BRONCHOFIBERVIDEOSCOPE

FDA UDI

OLYMPUS MEDICAL SYSTEMS CORP.·04953170399831·

EVIS EXERA II ULTRASONIC BRONCHOFIBERVIDEOSCOPE

FDA UDI

OLYMPUS MEDICAL SYSTEMS CORP.·04953170355608·

N/A

FDA UDI

HOYA CORPORATION·04961333225569·

Radiology Information Systems, Inc.

FDA UDI

Radiology Information Systems, Inc.·00860009490604·PowerDR Console Application is an X-ray digital...

VRPhysio

FDA UDI

XR HEALTH IL LTD·07290016986099·A software-only medical device intended for cer...

VRPhysio

FDA UDI

XR HEALTH IL LTD·07290016986082·A software-only medical device intended for upp...

VRCogni

FDA UDI

XR HEALTH IL LTD·07290016986075·A software-only medical device intended for mot...

Clear Guide CORE

FDA UDI

CLEAR GUIDE MEDICAL, INC.·B201CGCORE170·The device is intended as a computer platform t...

DIGITAL MEDICAL SCOPE

FDA UDI

NIDEK CO.,LTD.·04987669101070·The assembly system (control unit & DS-10EA Ada...

System, Test, Her-2/Neu, Ihc

FDA Pre-Market Approval

FDA Class 3 ·PATHWAY ANTI-HER-2/NEU (4B5) PRIMARY ANTIBODY