Reprocessed MyoSure REACH Tissue Removal Device

FDA registration

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

StrykerSustainability (GP) - Reprocessed MyoSure LITE Tissue Removal Device

FDA registration

Isomedix Operations Inc.·1 product·🇺🇸 United States

Reprocessed MyoSure REACH Tissue Removal Device

FDA registration

Stryker Sustainability Solutions·1 product·🇺🇸 United States

Reprocessed MyoSure REACH Tissue Removal Device

FDA registration

Stryker Sustainability Solutions - Chandler·1 product·🇺🇸 United States

Reprocessed MyoSure Tissue Removal Device, Reprocessed MyoSure REACH Tissue Removal Device, Reprocessed MyoSure LITE Tissue Removal Device, Reprocessed MyoSure XL Tissue Removal Device, Reprocessed MyoSure XL Tissue Removal Device for Fluent

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

Hysteroscope (And Accessories)

FDA classification

FDA Class 2 ·Hysteroscope (And Accessories)

HHM

FDA UDI

Oticon A/S·05707131351586·G500 SC, BTE PP 13 2.4G 105 C057 TAR HHM

METAPHYSARY BROACH ESOP LEFT SIZE 10

FDA UDI

FOURNITURES HOSPITALIERES INDUSTRIE·03661489017568·

NA

FDA UDI

Synthes GmbH·10886982142672·2.4MM CORTEX SCREW SLF-TPNG WITH T8 STARDRIVE R...

7450 RV2 MASK

FDA UDI

HANS RUDOLPH, INC.·00817136022543·7450M FACE MASK-HDGR & 2700 MA

MOZART SUPRA (XPERT84)

FDA registration

Kub Technologies, Inc.·1 product·🇺🇸 United States

Sleeve Cuff Kit

FDA registration

WELCH ALLYN, INC.·1 product·🇺🇸 United States

LOR Syringe

FDA registration

JIANGSU CAINA MEDICAL CO., LTD·1 product·🇨🇳 China

Medical Facets NC

FDA UDI

MEDICAL FACETS NC LLC·M933MDF2017560·2.4mm Cortex Screw, T8 Stardrive, Self-Tapping,...

WELCH ALLYN ABPM 6100

FDA 510(k)

FDA Class 2 ·Cardiovascular

LUNAR REPORT GENERATOR II

FDA 510(k)

FDA Class 2 ·Radiology

Densitometer, Bone

FDA classification

FDA Class 2 ·Densitometer, Bone

System, Measurement, Blood-Pressure, Non-Invasive

FDA classification

FDA Class 2 ·System, Measurement, Blood-Pressure, Non-Invasive