Automated External Defibrillators (Non-Wearable)

FDA Pre-Market Approval

FDA Class 3 ·QUIK-PAK Electrodes

Occluder, Patent Ductus, Arteriosus

FDA Pre-Market Approval

FDA Class 3 ·NIT-OCCLUD PDA

Automated External Defibrillators (Non-Wearable)

FDA Pre-Market Approval

FDA Class 3 ·QUIK-PAK™ Electrodes

Occluder, Patent Ductus, Arteriosus

FDA Pre-Market Approval

FDA Class 3 ·NIT-OCCLUD PDA

Occluder, Patent Ductus, Arteriosus

FDA Pre-Market Approval

FDA Class 3 ·NIT-OCCLUD PDA

Automated External Defibrillators (Non-Wearable)

FDA Pre-Market Approval

FDA Class 3 ·QUIK-PAK Electrodes

Solidlock Positioning

FDA registration

MTT GMBH·1 product·🇩🇪 Germany

BioJet

FDA registration

MTT GMBH·1 product·🇩🇪 Germany

TargetPro

FDA registration

MTT GMBH·1 product·🇩🇪 Germany

Wolf Endomotion System

FDA registration

MTT GMBH·1 product·🇩🇪 Germany

AESCULAP

FDA UDI

AESCULAP, INC.·04046955086597·, non-sterile, reusable

GROUP A STREPTOCOCCUS

FDA UDI

Hologic, Inc.·15420045506312·

THREADED CR-Ti

FDA UDI

MEDTRONIC SOFAMOR DANEK, INC.·00721902170645·7MM X 14MM THREADED CR-TI

N/A

FDA UDI

MEDTRONIC SOFAMOR DANEK, INC.·00885074000770·CEMENT RESTRICTOR X1203056 TCR 11 X 25

ShurFit CRT Peek Cage

FDA UDI

PRECISION SPINE, INC.·00840019908757·CRT Peek 5 degree x 5mm

GROUP A STREPTOCOCCUS

FDA UDI

Hologic, Inc.·15420045506305·

Integra® Jarit®

FDA UDI

INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780203032·Integra® Jarit® Braun Episiotomy Scissors, 8-3/4"

Cement Restrictor

FDA UDI

TECRES SPA·08031497001562·Cement Restrictor designed to be inserted into ...

ShurFit CRT Peek Cage

FDA UDI

PRECISION SPINE, INC.·00840019908887·CRT Peek 10 degree x 10mm

ShurFit ACIF Titanium

FDA UDI

PRECISION SPINE, INC.·00840019929233·ACIF Cage 5 degree x 6mm