20 results · 41ms · Sources: EU EUDAMED, US FDA

Genadyne Biotechnologies, Inc.

FDA registration
Genadyne Biotechnologies, Inc.·1 product·🇺🇸 United States

GENADYNE BIOTECHNOLOGIES, INC.

FDA registration
GENADYNE BIOTECHNOLOGIES, INC.·1 product·🇺🇸 United States

Nasal Pillow Mask - Small (NNPM-01/ Nefes S); Nasal Pillow Mask - Medium (NNPM-02/ Nefes M); Nasal Pillow Mask - Large (NNPM-03/ Nefes L)

FDA 510(k)
FDA Class 2 ·Anesthesiology

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772814282·GENUMEDI PT SILVER R V

QP-Prostate® CAD

FDA registration
QUIBIM S.L.·1 product·🇪🇸 Spain

QP-Brain®

FDA registration
QUIBIM S.L.·2 products·🇪🇸 Spain

QP-Prostate

FDA registration
QUIBIM S.L.·1 product·🇪🇸 Spain

TAPERLOC COMPLETE RASP/PROVISIONAL

FDA UDI
Biomet Orthopedics, LLC·00880304632578·

Vilex Power Accessory

FDA UDI
VILEX IN TENNESSEE, INC.·00841731122315·KWire .094 x 9" (2.4x225mm)

Scalpel, Ultrasonic, Reprocessed, Reprocessed Ultrasonic Scalpel

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

Scalpel, Ultrasonic, Reprocessed, Reprocessed Ultrasonic Scalpel

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

Scalpel, Ultrasonic, Reprocessed, Reprocessed Ultrasonic Scalpel

FDA registration
Sterigenics US LLC·1 product·🇺🇸 United States

Reprocessed Ultrasonic Scalpel

FDA registration
Stryker Sustainability Solutions Lakeland·1 product·🇺🇸 United States

INFX-8000V, Wireless Foot Switch

FDA registration
Canon Medical Systems Corporation·2 products·🇯🇵 Japan

GripTract-GI Endoscopic Tissue Manipulator

FDA registration
ACTUATED MEDICAL, INC.·1 product·🇺🇸 United States

INFX-8000V with Wireless Footswitch

FDA 510(k)
FDA Class 2 ·Radiology

VANGUARD REPROCESSED ULTRASONIC SCALPEL

FDA 510(k)
FDA Unclassified ·Unknown

Ventilator, Non-Continuous (Respirator)

FDA classification
FDA Class 2 ·Ventilator, Non-Continuous (Respirator)

Single-Use Reprocessed Ultrasonic Surgical Instruments

FDA classification
FDA Unclassified ·Single-Use Reprocessed Ultrasonic Surgical Instruments

Interventional Fluoroscopic X-Ray System

FDA classification
FDA Class 2 ·Interventional Fluoroscopic X-Ray System