20 results · 45ms · Sources: EU EUDAMED, US FDA

VS Series Vital Signs Monitors (Including VS 9/VS 8/VS 8A)

FDA registration
SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD.·1 product·🇨🇳 China

VS Series Vital Signs Monitors (Including VS 9/VS 8/VS 8A)

FDA registration
Shenzhen Mindray Bio-Medical Electronics Co.,LTD·1 product·🇨🇳 China

Vital Signs Monitors VS 8

FDA registration
MINDRAY DS USA, Inc.·1 product·🇺🇸 United States

VS 8 Vital Signs Monitor, VS 8A Vital Signs Monitor, VS 9 Vital Signs Monitor

FDA registration
Flextronics Manufacturing (Singapore) Pte Ltd·1 product·🇸🇬 Singapore

VS 8 Vital Signs Monitor, VS 8A Vital Signs Monitor, VS 9 Vital Signs Monitor

FDA 510(k)
FDA Class 2 ·Cardiovascular

Wet-Field® Eraser®

FDA UDI
Beaver-Visitec International, Inc.·30886158010549·25 GA Fine Tip

BD BBL™ Chocolate II Agar

FDA UDI
BECTON, DICKINSON AND COMPANY·10382902212673·BD BBL™ Chocolate II Agar

Adaptix Interbody System with Titan nanoLOCK Surface Technology

FDA registration
Sterigenics US, LLC·2 products·🇺🇸 United States

Adaptix™ Interbody System with Titan nanoLock™ Surface Technology

FDA registration
MEDTRONIC SOFAMOR DANEK USA, INC.·2 products·🇺🇸 United States

Adaptix™ Interbody System with Titan nanoLock™ Surface Technology

FDA registration
Medtronic Engineering and Innovation Center (MEIC)·2 products·🇮🇳 India

Hi-dop

FDA registration
Bistos co., ltd.·1 product·🇰🇷 South Korea

Adaptix™ Interbody System with Titan nanoLock™ Surface Technology

FDA registration
Titan Spine, a Division of Medtronic·2 products·🇺🇸 United States

Starlight Imaging Catheter

FDA registration
SPECTRAWAVE, INC.·4 products·🇺🇸 United States

E-Z Chek® Residual Chlorine Test Strips - K100-0101B

FDA registration
REPROCESSING PRODUCTS CORPORATION (RPC)·1 product·🇺🇸 United States

Sterile Disposable Syringe with Needle

FDA registration
JIANGSU KANGBAO MEDICAL EQUIPMENT CO., LTD·3 products·🇨🇳 China

Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

FDA classification
FDA Class 2 ·Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

Adaptix Interbody System with Titan nanoLOCK Surface Technology

FDA 510(k)
FDA Class 2 ·Orthopedic

BT-200V VASCULAR DOPPLER

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

System, Monitoring, Perinatal

FDA classification
FDA Class 2 ·System, Monitoring, Perinatal

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification
FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar