14 results · 27ms · Sources: EU EUDAMED, US FDA

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SPECTRONIC 501 & 601 - CLINICAL SPECTROPHOTOMETER

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

Shoreline ACS

FDA UDI
Seaspine Orthopedics Corporation·10889981124359·9mm, 4-Hole Anterior Plate

Plateau-X Spacer System

FDA UDI
Life Spine, Inc.·00190837011963·

RESOLVE HEMOGLOBIN KIT, JB-2 STAINING SYSTEM, MODELS FR-9120, FR-9400, FR-9360, FR-9367

FDA 510(k)
FDA Class 2 ·Hematology

ProTrack RF Anchor Wire

FDA 510(k)
FDA Class 2 ·Cardiovascular

VERSACROSS CONNECT LAAC ACCESS SOLUTION

FDA Adverse Event
Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DRE·April 6, 2023

Multiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06 PerkinElmer Part Number: 2117-004 Product Usage: Multiphor II Electrophoresis System is a versatile modular electrophoresis system for horizontal electrophoresis, isoelectric focusing, 2-D electrophoresis and electrophoretic transfer Note: The Multiphor II Electrophoresis System (Class I) is the platform used with the hemoglobin electrophoresis gel kit ( Class II) sold by PerkinElmer as the Resolve Hemoglobin Kit (K050709: Product code JJN). The RESOLVE Systems Hemoglobin kit (K050709) is designed to separate whole blood, cord blood or dried blood spot specimen for detection of normal and variant hemoglobins by isoelectric focusing.

FDA Enforcement
Class II ·Terminated·Perkinelmer Life Sciences, Inc.·July 12, 2017

Multiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06 PerkinElmer Part Number: 2117-004 Product Usage: Multiphor II Electrophoresis System is a versatile modular electrophoresis system for horizontal electrophoresis, isoelectric focusing, 2-D electrophoresis and electrophoretic transfer Note: The Multiphor II Electrophoresis System (Class I) is the platform used with the hemoglobin electrophoresis gel kit ( Class II) sold by PerkinElmer as the Resolve Hemoglobin Kit (K050709: Product code JJN). The RESOLVE Systems Hemoglobin kit (K050709) is designed to separate whole blood, cord blood or dried blood spot specimen for detection of normal and variant hemoglobins by isoelectric focusing.

FDA Recall
Terminated ·Perkinelmer Life Sciences, Inc.·Product code JJN·May 15, 2017

MALLINCKRODT

FDA Adverse Event
Injury ·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code BTR·November 20, 2012

ESTYLUS 1:5 CONTRA ANGLE ATTACHMENT

FDA Adverse Event
Malfunction ·DENTSPLY PROFESSIONAL·Product code EKX·March 19, 2014

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN, INC.·Product code MDS·October 1, 2010

VERSACROSS ACCESS SOLUTION

FDA Adverse Event
Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DXF·April 19, 2023

VERSACROSS ACCESS SOLUTION

FDA Adverse Event
Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DYB·April 20, 2023

VERSACROSS CONNECT LAAC ACCESS SOLUTION

FDA Adverse Event
Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DXF·April 25, 2023