39 results · 18ms · Sources: EU EUDAMED, US FDA

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The product is a handheld ultraviolet-C germicidal wand and contains a combination of five UV-A and UV-C LED lights. The product comes in two configurations: UV-C x 1; UV-A x 4, or UV-C x 2; UV-A x 3. The product has two peak emission wavelengths at 274 nm and 397 nm.

FDA Enforcement
Class II ·Ongoing·Uvlizer c/o RAIS INTERNATIONAL LLC·April 29, 2026

Delivery/C-Section, Sterile-Kits containing the Devon Light Glove Catalog Numbers/Description: 56479 7335-SMC C-Section Kit 31404851 7382-OTO2 Delivery Kit 52000076E 7339-ES C-SECTION DELUXE PACK 52000082E 7335-HUV DELIVERY KIT

FDA Enforcement
Class II ·Terminated·Covidien LLC·July 29, 2015

DR 800. Digital Radiography X-ray System.

FDA Enforcement
Class II ·Ongoing·Agfa N.V.·September 4, 2024

MNA-420 ENC HDMI, Material Number K9303311; cathode ray tube display

FDA Enforcement
Class II ·Completed·Barco N.V.·July 17, 2024

Signature TKA GDE/MDL Set 04-05 (Femur & Tibia) The Signature Patient-Specific Surgical Guides are intended to be used as part of the Signature Personalized Patient Care System. Lt is intended to be used as a guide during the surgical procedure for total and partial knee arthroplasty.

FDA Enforcement
Class II ·Terminated·Materialise N.V.·March 25, 2015

Signature Patient-Specific Surgical Guides; patient specific instruments used as a guide during surgical procedure for total and partial knee arthroplasty. Part of the Signature Personalized Patient Care System.

FDA Enforcement
Class II ·Terminated·Materialise N.V.·November 4, 2015

DX-D 600 Product Usage: The DX-D 600 system is a ceiling mounted General Radiography X-Ray imaging system used in hospitals, clinics and medical practices by physicists, radiographers and radiologists to make, process and view static X-Ray radiographic images of the skeleton (including skull, spinal column and extremities), chest, abdomen and other body parts on adult, pediatric or neonatal patients.

FDA Enforcement
Class II ·Terminated·Agfa N.V.·October 3, 2018

Optional MDRC-1119 Front Cover Attachment Kit for review display monitors. Product Usage: The product is an optional kit, intended to be attached in front of the LCD panel of a review display (MDRC-1119).

FDA Enforcement
Class II ·Terminated·Barco N.V.·December 12, 2018

PET Plates Coated Film-MONOMEDBV2S2- Radiographic Film REF: XJUB8, XJM73, XJUDD, XJM85, EKLYZ. Product Usage: Due to an inhomogeneous coating solution, pinholes can become visible in even dark images. Visibility of the pinholes varies as material from this coating run shows pinholes in different frequencies and intensities.

FDA Enforcement
Class III ·Terminated·Agfa N.V.·March 27, 2019

AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic Product Usage: The Agfa s DR 800 system is indicated for performing dynamic imaging examinations (fluoroscopy and/or rapid sequence) of the following an anatomies/procedures: positioning fluoroscopy procedures, gastro-intestinal examinations, urogenital tract examinations, and angiography. It is intended to replace fluoroscopic images obtained through image intensifier technology. In addition, the system is intended for project radiography of all body parts. The DR 800 is not intended for mammography applications.

FDA Enforcement
Class II ·Terminated·Agfa N.V.·August 7, 2019

AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic, Type number: 6010/200 - Product Usage: DR 800: Agfa s DR 800 system is indicated for performing dynamic imaging examinations (fluoroscopy and/or rapid sequence) of the following anatomies/procedures: positioning fluoroscopy procedures, gastro-intestinal examinations, urogenital tract examinations, and angiography. It is intended to replace fluoroscopic images obtained through image intensifier technology. In addition, the system is intended for project radiography of all body parts. The DR 800 is not intended for mammography applications

FDA Enforcement
Class II ·Terminated·Agfa N.V.·June 10, 2020

TRUMATCH Orthognathic - Full Bimaxillary Surgical Kit, Catalog Number SD980.001

FDA Enforcement
Class II ·Terminated·Materialise N.V.·March 25, 2020

TRUMATCH Orthognathics - Genioplasty Surgical Kit, Add-on, Catalog Number: SD980.013

FDA Enforcement
Class II ·Terminated·Materialise N.V.·March 25, 2020

AGFA Digital Radiography X- Ray system DR 800 with TomoSynthesis- a Tomographic X-ray system - Product Usage: TomoSynthesis is used to synthesize tomographic slices from a single tomographic sweep. The DR 800 is not intended for mammography applications

FDA Enforcement
Class II ·Terminated·Agfa N.V.·March 25, 2020

Match Point System The Match Point System is intended to by uses as a surgical instrument to assist in the intraoperative positioning of glenoid components used with total and reverse shoulder arthroplasty by referencing anatomic landmarks of the shoulder that are identifiable on preoperative CT-image scans.

FDA Enforcement
Class II ·Terminated·Materialise N.V.·September 2, 2020

ProPlan CMF Patient-Specific Guide, Mandible guides (3A & 3B)-Intended to guide the marking of bone and/or guide surgical instruments in mandibular and maxillofacial surgical procedures. Identification number: SD900.101

FDA Enforcement
Class II ·Completed·Materialise N.V.·August 9, 2023

Barco MDNC-3421 DISPLAY, DIAGNOSTIC RADIOLOGY

FDA Enforcement
Class II ·Terminated·Barco N.V.·March 10, 2021

MRI Biomet Pin Guide for Total Knee Arthroplasty (Zimmer Biomet Patient Specific Instruments (PSI)-- patient-matched device designed to fit the patients anatomy to transfer a patient-specific pre-operative plan to the OR. Ref: KNM-ZB02-00-01

FDA Enforcement
Class II ·Completed·Materialise N.V.·July 26, 2023

Barco MDSC-8527 NXF, Part Number K9352421

FDA Enforcement
Class II ·Ongoing·Barco N.V.·February 14, 2024

Agfa DX-D 100 system-Digital Radiography mobile X-ray System. A mobile X-Ray modality, consisting of X-Ray console, generator, tube, digital detector, and workstation. This modality is used to generate projection X-Ray images of human patients. Models: 5411/ 050, A5411/ 0300 and A5411/ 0400

FDA Enforcement
Class II ·Ongoing·Agfa N.V.·April 10, 2024