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25-Hydroxy Vitamin D EIA, Catalog #AC-57F1. Product Usage: The IDS 25-Hydroxy Vitamin D EIA kit is an enzymeimmunoassay intended for the quantitative determination of 25-hydroxyvitamin D (25-OH D) and other hydroxylated metabolites in human serum or plasma. Results are to be used in conjunction with other clinical and laboratory data to assist the clinician in the assessment of vitamin D sufficiency in adult populations.

FDA Enforcement
Class II ·Terminated·IDS (Immunodiagnostic Systems Ltd.)·January 23, 2013

LEGION(R) TIB CONE IMPACTOR HEADS: a) REF 71441972, ID 24MM b) REF 71441971, ID 22MM c) REF 71441973, ID 26MM d) REF 71441974, ID 28MM e) REF 71441975, ID 30MM

FDA Enforcement
Class II ·Terminated·Smith & Nephew, Inc.·July 5, 2017

Histoplasma Immunodiffusion (ID) Antigen; The IFU labeling is for multiple products which included Fungal Antigens, Positive Controls and ID Plates,and Immunodiffusion (ID) Plates for use in the ID Test, Histoplasma ID Antigen

FDA Enforcement
Class II ·Terminated·Immuno-Mycologics, Inc·June 17, 2020

IDS-iSYS Ostase¿ BAP (Bone Alkaline Phosphatase) Control Set, Catalog Number IS-2830. Packaged in cardboard Box containing plastic bottles. The IDS-iSYS Ostase¿ BAP (IDS-iSYS BAP) Control Set is used for quality control of the IDS-iSYS Ostase¿ BAP (Bone Alkaline Phosphatase) Assay on the IDS-iSYS Multi-Discipline Automated Analyser.

FDA Enforcement
Class II ·Terminated·Immunodiagnostics Systems Ltd·October 17, 2012

LEGION(R) FEM CONE IMPACTOR HEADS: a) REF 71441976, ID 18MM b) REF 71441977, ID 20MM c) REF 71441978, ID 22MM

FDA Enforcement
Class II ·Terminated·Smith & Nephew, Inc.·July 5, 2017

IDS-iSYS N-Mid¿ Osteocalcin, Catalog Number IS-2930. Packaged in cardboard Box containing plastic bottles. The IDS-iSYS N-Mid¿ Osteocalcin Control Set is used for quality control of the IDS-iSYS N-Mid¿ Osteocalcin Assay on the IDS-iSYS Multi-Discipline Automated Analyser.

FDA Enforcement
Class II ·Terminated·Immunodiagnostics Systems Ltd·October 17, 2012

IDS-iSYS Intact PINP Control Set, Catalog Number IS-4030. Packaged in cardboard Box containing plastic bottles. The IDS-iSYS Intact amino-terminal propeptide of type I procollagen (Intact PINP) Control Set is used for quality control of the IDS-iSYS Intact PINP Assay on the IDS-iSYS Multi-Discipline Automated Analyser.

FDA Enforcement
Class II ·Terminated·Immunodiagnostics Systems Ltd·October 17, 2012

Superset with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy Port, REF 3503031. Airway connector.

FDA Enforcement
Class II ·Terminated·Intersurgical Inc·January 15, 2020

Superset with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy Port, REF 3521000. Airway connector.

FDA Enforcement
Class II ·Terminated·Intersurgical Inc·January 15, 2020

OptraPol Polishing Discs, Rx ONLY: OptraPol Refill Cup /10: REF/Product ID 634459, OptraPol Refill Small Flame/10: REF/Product ID 634458, OptraPol Assortment: REF/Product ID 634464 --Device Listing # B106952. One step polishing system for all common dental composites and amalgam.

FDA Enforcement
Class II ·Terminated·Ivoclar Vivadent, Inc.·August 17, 2016

IDS-iSYS Intact PINP, Catalog Number IS-4000. Packaged in cardboard Box containing plastic bottles. The IDS-iSYS Intact amino-terminal propeptide of type I procollagen (Intact PINP) assay is intended for the quantitative determination of intact PINP in human serum or plasma on the IDS-iSYS Multi-Discipline Automated Analyser.

FDA Enforcement
Class II ·Terminated·Immunodiagnostics Systems Ltd·October 17, 2012

IDS-iSYS Ostase¿ BAP (Bone Alkaline Phosphatase), Catalog Number IS-2800. Packaged in cardboard Box containing plastic bottles. The IDS-iSYS Ostase¿ BAP Assay (IDS-iSYS BAP) is intended for the quantitative determination of bone-specific alkaline phosphatase (BAP), an indicator of osteoblastic activity, in human serum or plasma on the IDS-iSYS Multi- Discipline Automated Analyser (Analyser). Results are to be used in conjunction with other clinical and laboratory data to aid the clinician in the management of post menopausal osteoporosis and Pagets disease.

FDA Enforcement
Class II ·Terminated·Immunodiagnostics Systems Ltd·October 17, 2012

Discovery NM 630 Model # H3101RH

FDA Enforcement
Class II ·Terminated·GE Healthcare, LLC·September 30, 2020

NM 830 Model # H3910AC

FDA Enforcement
Class II ·Terminated·GE Healthcare, LLC·September 30, 2020

NM/CT 850 Model Number: H3907AD

FDA Enforcement
Class II ·Terminated·GE Healthcare, LLC·September 30, 2020

NM/CT 870 DR Model # H3100AS

FDA Enforcement
Class II ·Terminated·GE Healthcare, LLC·September 30, 2020

bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is an automated system consisting of instruments, software and reagent cards designed for the ID and antimicrobial susceptibility testing of bacteria and yeast.

FDA Enforcement
Class II ·Terminated·Biomerieux Inc·August 29, 2018

Discovery 670 DR Model # H3100BT

FDA Enforcement
Class II ·Terminated·GE Healthcare, LLC·September 30, 2020

NM/CT 870 CZT Model # H3906CW

FDA Enforcement
Class II ·Terminated·GE Healthcare, LLC·September 30, 2020

QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator; QUADROX-i ADULT HMO 70000 / HMO 71000; QUADROX-iD Pediatric HMOD 30000. The QUADROX oxygenators are intended for use in extracorporeal circulation during cardiopulmonary bypass in cardiac surgery.

FDA Enforcement
Class II ·Terminated·Maquet Cardiovascular Us Sales, Llc·October 2, 2013