PLEGIOX Cardioplegia Heat Exchanger

FDA UDI

Maquet Cardiopulmonary AG·04037691229591·PLEGIOX Heat Exchanger, SOFTLINE coated, Steril...

Capiox® FX Advance Hollow Fiber Oxygenator w Integrated AF w Hardshell Res.

FDA UDI

Terumo Cardiovascular Systems Corporation·00699753450820·

Curaplex

FDA UDI

BOUND TREE MEDICAL, LLC·00815277021500·FBI m9 Medical Refill Kit 2014

Capiox® FX Advance Hollow Fiber Oxygenator w Integrated AF w Hardshell Res.

FDA UDI

Terumo Cardiovascular Systems Corporation·00699753450837·

NA

FDA UDI

Maquet Cardiopulmonary AG·04037691873077·Holding Clamp for Oxygenator QUADROX-iR

Capiox® FX Hollow Fiber Oxygenator w Integrated Arterial Filter w Hardshell Res.

FDA UDI

Terumo Cardiovascular Systems Corporation·00699753450462·

Capiox® FX Advance Hollow Fiber Oxygenator w Integrated AF w Hardshell Res.

FDA UDI

Terumo Cardiovascular Systems Corporation·00699753450783·

Capiox® FX Hollow Fiber Oxygenator w Integrated Arterial Filter w Hardshell Res.

FDA UDI

Terumo Cardiovascular Systems Corporation·00699753450448·

Capiox® FX Advance Hollow Fiber Oxygenator w Integrated AF w Hardshell Res.

FDA UDI

Terumo Cardiovascular Systems Corporation·00699753450806·

Capiox® FX Hollow Fiber Oxygenator w Integrated Arterial Filter w Hardshell Res.

FDA UDI

Terumo Cardiovascular Systems Corporation·00699753450752·

Curaplex

FDA UDI

BOUND TREE MEDICAL, LLC·00815277020855·Curaplex Advance Oxy Kit

Capiox® FX Hollow Fiber Oxygenator w Integrated Arterial Filter w Hardshell Res.

FDA UDI

Terumo Cardiovascular Systems Corporation·00699753450745·

Capiox® FX Advance Hollow Fiber Oxygenator w Integrated AF w Hardshell Res.

FDA UDI

Terumo Cardiovascular Systems Corporation·00699753450813·

ATM/p53/13q14/RB1/CSP12 gene Probe Detection Kit (fluorescence in situ hybridization )

Basic UDI-DI

EU IVDD · Eu Ivd General ·Wuhan YZY Medical Science and Technology Co., Ltd·1 device

FI20/07011

Certificate

MDD Annex II (excluding section 4)·QT Medical, Inc.·SGS FIMKO OY·1 Basic UDI-DI

QMT-Tech ab

System producer

🇸🇪 Sweden

Kidney Perfusion Kit

FDA classification

FDA Class 2 ·Kidney Perfusion Kit

Parenteral Administration Kit

FDA classification

FDA Class 2 ·Parenteral Administration Kit

D And C Tray

FDA classification

FDA Not Classified ·D And C Tray

Remote Or Wearable Patient Monitoring Device For Drug Induced Qt Prolongation Monitoring

FDA classification

FDA Not Classified ·Remote Or Wearable Patient Monitoring Device For Drug Induced Qt Prolongation Monitoring