21 results · 47ms · Sources: EU EUDAMED, US FDA

MEGA 7.5FR. 30cc Intra-Aortic Balloon Catheter & Accessories

FDA registration
Datascope Corp·1 product·🇺🇸 United States

MEGA 7.5FR. 30cc Intra-Aortic Balloon Catheter & Accessories

FDA registration
Datascope Corp.·1 product·🇺🇸 United States

MEGA(TM) 7.5FR. 30CC INTRA-AORTIC BALLOON CATHETER AND ACCESSORIES, MEGA(TM) 7.5FR. 40CC INTRA-AORTIC BALLOON CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

SYNTHES MATRIX SYSTEM; K120838

FDA registration
EXEL INC. DBA DHL SUPPLY CHAIN (USA)·5 products·🇺🇸 United States

System, Balloon, Intra-Aortic And Control

FDA classification
FDA Class 2 ·System, Balloon, Intra-Aortic And Control

JARVIS SURGICAL INC.

FDA registration
JARVIS SURGICAL INC.·2 products·🇺🇸 United States

ITOTAL CRUCIATE RETAINING IJIG ANCILLARY INSTRUMENTS

FDA registration
ConforMIS, Inc.·2 products·🇺🇸 United States

PPD MEDITECH, DIV. OF INDUSTRIES PPD INC.

FDA registration
PPD MEDITECH, DIV. OF INDUSTRIES PPD INC.·1 product·🇨🇦 Canada

Cashmere Non -Sterile Powder free Nitrile exam gloves- White

FDA registration
MAXTER HEALTHCARE INC·1 product·🇺🇸 United States

Hayden Medical

FDA UDI
Hayden Medical, Inc.·00840319704110·Bishop-Harmon Tissue Forceps 3-3/8" (8.6cm), st...

Cleerly Ischemia

FDA UDI
CLEERLY, INC.·00860001924121·Cleerly ISCHEMIA is an add-on software module t...

Amphenol (Changzhou) Connector Systems Co., Ltd.

FDA registration
Amphenol (Changzhou) Connector Systems Co., Ltd.·1 product·🇨🇳 China

RICHARD WOLF GMBH

FDA registration
RICHARD WOLF GMBH·1 product·🇩🇪 Germany

Thermometrics Mexico, S.A. de C.V

FDA registration
Thermometrics Mexico, S.A. de C.V·1 product·🇲🇽 Mexico

RICHARD WOLF MEDICAL INSTRUMENTS CORP.

FDA registration
RICHARD WOLF MEDICAL INSTRUMENTS CORP.·1 product·🇺🇸 United States

AMID Stapler or AMID Hernia Fixation Device

FDA registration
Sterigenics US LLC·2 products·🇺🇸 United States

CASHMERE NON-STERILE, POWDER FREE NITRILE EXAMINATION GLOVES (WHITE)

FDA 510(k)
FDA Class 1 ·General Hospital

CONFORMIS ITOTAL CR KNEE REPLACEMENT SYSTEM (KRS)

FDA 510(k)
FDA Class 2 ·Orthopedic

1120720

FDA registration
CORIN LTD.·1 product·🇬🇧 United Kingdom

Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

FDA classification
FDA Class 2 ·Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer