20 results · 48ms · Sources: EU EUDAMED, US FDA

SeraQuest Anti-Cardiolipin IgG

FDA registration
QUEST INTL., INC.·1 product·🇺🇸 United States

ANTI-CARDIOLIPIN, MULTIPLE AUTOANTIBODIES IMMUNOLOGICAL TEST SYSTEM

FDA 510(k)
FDA Class 2 ·Immunology

System, Test, Anticardiolipin Immunological

FDA classification
FDA Class 2 ·System, Test, Anticardiolipin Immunological

SYNTHES USS (10MM SIDE OPENING SCREWS); K003061

FDA registration
EXEL INC. DBA DHL SUPPLY CHAIN (USA)·4 products·🇺🇸 United States

ZEVO™ Anterior Cervical Plate System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169329560·PLATE 3003069 ZEVO 69MM 3 LVL

Safety Blood Collection Set

FDA registration
MERCEDES MEDICAL LLC·1 product·🇺🇸 United States

VACUFLOW+ BLOOD COLLECTION SET, MODEL 52221/3/5

FDA registration
ANHUI HONGYU WUZHOU MEDICAL MANUFACTURER CO., LTD.·1 product·🇨🇳 China

Synergy Sterilisation (M) Sdn Bhd

FDA registration
Synergy Sterilisation (M) Sdn Bhd·1 product·🇲🇾 Malaysia

GRAND TEN HOLDINGS SDN BHD

FDA registration
GRAND TEN HOLDINGS SDN BHD·1 product·🇲🇾 Malaysia

Biotroni Bio-Guard Slide Safety Blood Collection Set with Pre-Attached Holder

FDA registration
BIOTRONIX HEALTHCARE INDUSTRIES INC.·1 product·🇺🇸 United States

WRP ASIA PACIFIC SDN. BHD.

FDA registration
WRP ASIA PACIFIC SDN. BHD.·1 product·🇲🇾 Malaysia

Unicondylar Interpostitional Spacer

FDA registration
ZIMMER, INC.·1 product·🇺🇸 United States

N-MID® Osteocalcin ELISA

FDA registration
IMMUNODIAGNOSTIC SYSTEMS LTD.·1 product·🇬🇧 United Kingdom

UNICONDYLAR INTERPOSITIONAL SPACER

FDA registration
Sterigenics US, LLC·1 product·🇺🇸 United States

N-MID® Osteocalcin ELISA

FDA registration
EUROIMMUN US INC.·1 product·🇺🇸 United States

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523132508·3-Level Anterior Cervical Plate, 69mm

VACUFLOW+ BLOOD COLLECTION SET, MODEL 52221/3/5; VACUFLOW+ WITH HOLDER BLOOD COLLECTION SET, MODEL 82021/3/5 WITH HOLDER

FDA 510(k)
FDA Class 2 ·General Hospital

MODEL 4000 EEG MONITOR WITH PSI (PSA4000)

FDA 510(k)
FDA Class 2 ·Neurology

Index-Generating Electroencephalograph Software

FDA classification
FDA Class 2 ·Index-Generating Electroencephalograph Software

Needle, Hypodermic, Single Lumen

FDA classification
FDA Class 2 ·Needle, Hypodermic, Single Lumen