11 results · 17ms · Sources: EU EUDAMED, US FDA

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PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.

FDA Recall
Terminated ·Biomerieux Inc·Product code LXG·August 28, 2012

WASP (Walk Away Specimen Process). Automatic Planting and Streaking Instrument Catalog number: W086 WASP is a fully automated system used to process microbiological specimens in liquid phase for the investigation of infectious microbes.

FDA Recall
Terminated ·Copan Italia Via Perotti, 10 Brescia Italy·Product code JTC·August 9, 2013

Neos Vanadium Excavator Part Number 591/0 SCHE

FDA Recall
Terminated ·Sybron Dental Specialties·Product code EKC·November 14, 2008

Neos Vanadium Excavator Part Number 591/0-6

FDA Recall
Terminated ·Sybron Dental Specialties·Product code EKC·November 14, 2008

Neos Vanadium Excavator Part Number 591/3 SCHE

FDA Recall
Terminated ·Sybron Dental Specialties·Product code EKC·November 14, 2008

Neos Vanadium Excavator Part Number 591/4

FDA Recall
Terminated ·Sybron Dental Specialties·Product code EKC·November 14, 2008

Neos Vanadium Excavator Part Number 591/5 SCHE

FDA Recall
Terminated ·Sybron Dental Specialties·Product code EKC·November 14, 2008

Neos Vanadium Excavator Part Number 591/2

FDA Recall
Terminated ·Sybron Dental Specialties·Product code EKC·November 14, 2008

Neos Vanadium Excavator Part Number 591/0

FDA Recall
Terminated ·Sybron Dental Specialties·Product code EKC·November 14, 2008

Neos Vanadium Excavator Part Number 591/1

FDA Recall
Terminated ·Sybron Dental Specialties·Product code EKC·November 14, 2008

T-Handle, Strike Plate, Push Connection, Part Number: SI50023 Rev A T-handles are silicone handled instruments that have a quick release end. The silicone T-handle has an impactor cap on the proximal end of the handle which is designed to be struck with a mallet. T-handles are used primarily to attach to, and operate a wide range of instruments used during implantation of spinal intervertebral body fusion devices intended for intervertebral body fusion of the spine of skeletally mature patients.

FDA Recall
Terminated ·SpineFrontier, Inc.·Product code MDM·August 29, 2012