20 results
·
58ms
·
Sources: EU EUDAMED, US FDA
STA - Unicalibrator
FDA registration
DIAGNOSTICA STAGO, INC.·1 product·🇺🇸 United States
STA - Unicalibrator
FDA registration
Diagnostica Stago - Taverny·1 product·🇫🇷 France
STA - Unicalibrator
FDA registration
Diagnostica Stago - Taverny·1 product·🇫🇷 France
UNICALIBRATOR KIT
FDA 510(k)
FDA Class 2
·Hematology
Plasma, Control, Normal
FDA classification
FDA Class 2
·Plasma, Control, Normal
LEONE SPA
FDA UDI
LEONE SPA·08033707059868·DB BRACKETS 21 EXTREMO NO-Ni 22 T+12A+5
75V - Class A 21 - 3 Shelf Cabinet
FDA UDI
Certified Safety Manufacturing, Inc.·00766588620213·75V - Class A 21 - 3 Shelf Cabinet
Partial Thromboplastin (APT) Reagent
FDA registration
SANZAY CORPORATION -·1 product·🇺🇸 United States
ACTIVATED PARTIAL THROMBOPLASTIN
FDA registration
TECO DIAGNOSTICS·1 product·🇺🇸 United States
Synergy Health Marseille SAS
FDA registration
Synergy Health Marseille SAS·1 product·🇫🇷 France
STERISPINE LC Lumbar Interbody Device
FDA registration
SAFE ORTHOPAEDICS SAS·1 product·🇫🇷 France
QuickCoag APTT-EA
FDA registration
BIOMEDICA DIAGNOSTICS INC.·1 product·🇨🇦 Canada
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668113189·STERILIZING CASE SMALL KATENA IOP
VITAL SCIENTIFIC APTT, APTT & QUIKCOAG APTT
FDA 510(k)
FDA Class 2
·Hematology
STERISPINE LC CAGE
FDA 510(k)
FDA Class 2
·Orthopedic
ZMR®
FDA UDI
Zimmer, Inc.·00889024157163·
ZMR®
FDA UDI
Zimmer, Inc.·00889024157187·
ZMR®
FDA UDI
Zimmer, Inc.·00889024157170·
Activated Partial Thromboplastin
FDA classification
FDA Class 2
·Activated Partial Thromboplastin
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar