20 results · 44ms · Sources: EU EUDAMED, US FDA

VERIFY Self-Contained Biological Indicator HP Activator (LCB004) (PC-SD)

FDA registration
STERIS CORPORATION·1 product·🇺🇸 United States

VERIFY V24 SELF-CONTAINED BIOLOGICAL INDICATOR

FDA 510(k)
FDA Class 2 ·General Hospital

GYRUS ACMI, INC

FDA UDI
Gyrus Acmi, Inc.·00821925017016·RICHARDS RIBBON LOOP 5.25 MM LENGTH PLATINUM

Indicator, Biological Sterilization Process

FDA classification
FDA Class 2 ·Indicator, Biological Sterilization Process

GEN4 INTERACTIVE

FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828158930·GEN4 INTERACTIVE

GEN4 Direct Access

FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828127417·GEN4 Direct Access

Equinoxe Reverse Shoulder Superior Augment Glenoid Plate

FDA registration
Exactech Sarasota·3 products·🇺🇸 United States

Equinoxe Reverse Shoulder Superior Augment Glenoid Plate

FDA registration
EXACTECH, INC.·3 products·🇺🇸 United States

Isomedix Operations, Inc.

FDA registration
Isomedix Operations, Inc.·3 products·🇺🇸 United States

Poly stat Strep A Flip Test

FDA registration
POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC.·1 product·🇺🇸 United States

BioSign Strep A Flip

FDA registration
PRINCETON BIOMEDITECH CORP.·1 product·🇺🇸 United States

ISOMEDIX OPERATIONS INC.

FDA registration
ISOMEDIX OPERATIONS INC.·3 products·🇺🇸 United States

Foot Osteotomy Wedge System

FDA UDI
Tyber Medical LLC·M6951407080·CerviFuse Lordotic Spacer, 11 x 14 x 8mm

Suzhou Armocon Technology Co., Ltd.

FDA registration
Suzhou Armocon Technology Co., Ltd.·1 product·🇨🇳 China

Colistin Disk

FDA registration
REMEL EUROPE LTD·1 product·🇬🇧 United Kingdom

LELO USA INC.

FDA registration
LELO USA INC.·1 product·🇺🇸 United States

STATUS FIRST STREP A

FDA 510(k)
FDA Class 1 ·Microbiology

PIONEER ANTERIOR CERVICAL PLATE MODEL 24-SERIES

FDA 510(k)
FDA Class 2 ·Orthopedic

Antigens, All Groups, Streptococcus Spp.

FDA classification
FDA Class 1 ·Antigens, All Groups, Streptococcus Spp.

Appliance, Fixation, Spinal Intervertebral Body

FDA classification
FDA Class 2 ·Appliance, Fixation, Spinal Intervertebral Body