NKX3.1

FDA UDI

BIOCARE MEDICAL LLC·00847627008022·

Rabbit Monoclonal Anti-Human NKX3.1 Antibody, EP356

FDA UDI

Epitomics Inc.·00810113068343·Rabbit Monoclonal Anti-Human NKX3.1 (356),conce...

NKX3.1 [D2Y1A]

FDA UDI

BIOCARE MEDICAL LLC·00847627025784·

Rabbit Monoclonal Anti-Human NKX3.1 Antibody, EP356

FDA UDI

Epitomics Inc.·00810113068329·Rabbit Monoclonal Anti-Human NKX3.1 (356), 0.1 ...

NKX2.2 RMab

FDA UDI

BIO SB, INC.·B502BSB31090·NKX2.2 is a rabbit monoclonal antibody derived ...

Tissue-Tek Genie®

FDA UDI

SAKURA FINETEK U.S.A., INC.·00615233007445·anti-NKX3.1 Rabbit Monoclonal Antibody [EP356],...

NKX2.2 (EP336) Rabbit Monoclonal Primary Antibody

FDA UDI

CELL MARQUE CORPORATION·00841683144571·

Tinto NKX2.2 RMab

FDA UDI

BIO SB, INC.·B502BSB31070·NKX2.2 is a rabbit monoclonal antibody derived ...

NKX2.2 RMab

FDA UDI

BIO SB, INC.·B502BSB31110·NKX2.2 is a rabbit monoclonal antibody derived ...

Recaro Monza CFX Reha

Device

EU MDR · Eu Md Class 1 ·Thomas Hilfen für Körperbehinderte GmbH & Co. Medico KG·On the market

PRO-PICC® CT (6F X 60CM TRIPLE)

FDA registration

MARTECH MEDICAL PRODUCTS S. DE RL. DE CV.·1 product·🇲🇽 Mexico

cannula, plastic surgery

FDA registration

FX MACHINE·1 product·🇺🇸 United States

COMPASS ™

FDA UDI

B BRAUN INTERVENTIONAL SYSTEMS, INC·04046955668847·4F X 45CM HEMO STRAIGHT

SUPER SHEATH 2.0SUPER SHEATH 2.0

FDA UDI

Medical Components, Inc.·00884908100235·3F X 10CM PTFE TEARAWAY

COMPASS ™

FDA UDI

B BRAUN INTERVENTIONAL SYSTEMS, INC·04046955668823·4F X 15CM HEMO STRAIGHT

SUPER SHEATH 2.0SUPER SHEATH 2.0

FDA UDI

Medical Components, Inc.·00884908093636·3F X 5CM PTFE TEARAWAY

COMPASS ™

FDA UDI

B BRAUN INTERVENTIONAL SYSTEMS, INC·04046955668861·4F X 60CM HEMO STRAIGHT

COMPASS ™

FDA UDI

B BRAUN INTERVENTIONAL SYSTEMS, INC·04046955668885·4F X 90CM HEMO STRAIGHT

SUTURE LOCK NAIL BONE ANCHOR WITH WHITE (KFX-W-200) & BLUE (KFX-B-200) FIBERFORCE SUTURE

FDA 510(k)

FDA Class 2 ·Orthopedic

AFX MICROWAVE GENERATOR, FLEX ABLATION WAND, LYNX ABLATION WAND, MODEL SERIES 1000, P/N 102006, P/N 102007

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery