SYNTHES CERVIFIX SYSTEM; K011969

FDA registration

EXEL INC. DBA DHL SUPPLY CHAIN (USA)·1 product·🇺🇸 United States

SYNTHES CERVIFIX SYSTEM

FDA registration

Synthes (USA) Products LLC·1 product·🇺🇸 United States

Jabil Inc. (Brandywine)

FDA registration

Jabil Inc. (Brandywine)·1 product·🇺🇸 United States

APPLIANCE, FIXATION, SPINAL INTERLAMINAL

FDA registration

SYNTHES GMBH·1 product·🇨🇭 Switzerland

SYNTHES CERVIFIX SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

K011968

FDA registration

Lake Region Medical·1 product·🇺🇸 United States

UltraSafe Passive Needle Guard

FDA registration

BECTON DICKINSON·1 product·🇺🇸 United States

LiquidQC hsCRP Controls

FDA registration

CLINIQA CORPORATION·1 product·🇺🇸 United States

Merit Medical®

FDA UDI

Merit Medical Systems, Inc.·00884450202920·

Anti-Desmoglein 1 ELISA (IgG)

FDA registration

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

Anti-Desmoglein 3 ELISA (IgG)

FDA registration

EUROIMMUN Medizinische Labordiagnostika AG·1 product·🇩🇪 Germany

JW-120B

FDA registration

NIHON KOHDEN AMERICA, INC.·1 product·🇺🇸 United States

JW-120B

FDA registration

NIHON KOHDEN CORP.·1 product·🇯🇵 Japan

Anti-Desmoglein 3 ELISA (IgG)

FDA registration

EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG·1 product·🇩🇪 Germany

NEURO N100 RADIOFREQUENCY GENERATOR AND ACCESSORY CABLES

FDA 510(k)

FDA Class 2 ·Neurology

GT2 FUSION GUIDE WIRE, MODEL NTLHLJ180,NTLHLS180, NTLHLJ300, NTLHLS300

FDA 510(k)

FDA Class 2 ·Cardiovascular

Appliance, Fixation, Spinal Interlaminal

FDA classification

FDA Class 2 ·Appliance, Fixation, Spinal Interlaminal

Generator, Lesion, Radiofrequency

FDA classification

FDA Class 2 ·Generator, Lesion, Radiofrequency

Catheter, Percutaneous

FDA classification

FDA Class 2 ·Catheter, Percutaneous