LOQTEQ Distal Medial Tibia 3.5 System

FDA registration

AAP IMPLANTATE AG·2 products·🇩🇪 Germany

AAP LOQTEQ DISTAL MEDIAL TIBIA PLATE 3.5 SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

SimplyGo Mini

FDA UDI

Respironics, Inc.·00606959032392·SimplyGo Mini with Standard Battery, USA

N/A

FDA UDI

HANS RUDOLPH, INC.·00874750003877·75 V2 MED 22OD STRAIGHT NO HG

CATHETER, PERCUTANEOUS

FDA registration

Cosmed Group Inc.·1 product·🇺🇸 United States

MyCardia AT

FDA registration

Datrix LLC·1 product·🇺🇸 United States

Electrocardiograph, ambulatory (without analysis)

FDA registration

ACS Diagnostics, INC.·1 product·🇺🇸 United States

Mercodia C-peptide ELISA

FDA UDI

Mercodia AB·07350108630085·Mercodia C-peptide ELISA provides a method for ...

GLOBALMED INTERNATIONAL LTD

FDA registration

GLOBALMED INTERNATIONAL LTD·1 product·🇭🇰 Hong Kong

BIOPLEX 2200 ANA SCREEN RE Detector Cleaning Pack

FDA registration

BIO-RAD LABORATORIES, INC.·1 product·🇺🇸 United States

NUMED MULLINS PTA CATHETER

FDA 510(k)

FDA Class 2 ·Cardiovascular

AUDIT MICROCV IMMUNOASSAY LINEARITY SET

FDA 510(k)

FDA Class 1 ·Clinical Chemistry

Plate, Fixation, Bone

FDA classification

FDA Class 2 ·Plate, Fixation, Bone

Multi-Analyte Controls, All Kinds (Assayed)

FDA classification

FDA Class 1 ·Multi-Analyte Controls, All Kinds (Assayed)

Catheter, Percutaneous

FDA classification

FDA Class 2 ·Catheter, Percutaneous