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