12 Fr. Two-Lumen Hemodialysis Catheterization Kit/Set with Blue FlexTip Catheter

FDA registration

RHENUS SE & CO. KG·1 product·🇩🇪 Germany

Two-Lumen Hemodialysis Catheterization Kit/Set with Blue FlexTip Catheter

FDA registration

Arrow International CR, a.s.·1 product·🇨🇿 Czechia

Arrow® Marked Spring-Wire Guide with Arrow Advancer¿

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

Two-Lumen Hemodialysis Catheterization Kit/Set with Blue FlexTip Catheter

FDA registration

Arrow International C.R. a.s.·1 product·🇨🇿 Czechia

Two-Lumen Hemodialysis Catheterization Kit/Set with Blue FlexTip Catheter

FDA registration

Teleflex LLC (NADC 2)·1 product·🇺🇸 United States

12 Fr Heparin Two-Lumen Hemodialysis Catheterization Kit/Set

FDA registration

Teleflex Medical LLC·1 product·🇺🇸 United States

12 Fr Heparin Two-Lumen Hemodialysis Catheterization Kit/Set

FDA registration

Teleflex LLC (NADC)·1 product·🇺🇸 United States

Two-Lumen Hemodialysis Catheterization Kit/Set with Blue FlexTip Catheter

FDA registration

Arrow Internacional de Chihuahua S.A. de C.V.·1 product·🇲🇽 Mexico

Arrow® Marked Spring-Wire Guide with Arrow Advancer¿

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

STERIS AST CZ s.r.o.

FDA registration

STERIS AST CZ s.r.o.·1 product·🇨🇿 Czechia

ARROW LARGE-BORE DUAL LUMEN HEMODIALYSIS KIT

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

Catheter, Subclavian

FDA classification

FDA Class 2 ·Catheter, Subclavian

HTO Staple

FDA registration

HOWMEDICA OSTEONICS CORP·1 product·🇺🇸 United States

KOSSAN LATEX INDUSTRIES (M) SDN BHD

FDA registration

KOSSAN LATEX INDUSTRIES (M) SDN BHD·1 product·🇲🇾 Malaysia

ALMARK TOOL & MANUFACTURING COMPANY, INC.

FDA registration

ALMARK TOOL & MANUFACTURING COMPANY, INC.·1 product·🇺🇸 United States

ISOMEDIX OPERATIONS INC.

FDA registration

ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States

Stry Mah

FDA registration

Phillips Precision Inc·1 product·🇺🇸 United States

ISOMEDIX OPERATIONS INC.

FDA registration

ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States

Arthrex®

FDA UDI

ARTHREX, INC.·00888867133594·JOYSTICK, PERCUTANEOUS GUIDE

PATIENT EXAMINATION GLOVES (LATEX)

FDA 510(k)

FDA Class 1 ·General Hospital