BEUDAMED
    21 results · 13ms · Sources: EU EUDAMED, US FDA

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    Procedural kits containing ultrasonic transmission gel, Item Numbers: a) 28-EG103, b) 28-EG125, c) 28-EG135, d) 28-EG151, e) 28-EG161, f) 28-EG163, g) 28-EG197

    FDA Recall
    Open, Classified ·Advance Medical Designs, Inc.·Product code GDF·July 7, 2023

    procedural kits containing ultrasonic transmission gel, Item Numbers: a) 28-GG023, b) 28-GG105, c) 28-GG107, d) 28-GG121, e) 28-GG219, f) 28-GG223, g) 28-GG303, h) 28-GG307, i) 28-GG519, j) 28-GG519PC, k) 28-GG521, l) 28-GG521PC, m) 28-GG529, n) 28-GG553, o) 28-GG569, p) 28-GG571, q) 28-GG723

    FDA Recall
    Open, Classified ·Advance Medical Designs, Inc.·Product code GDF·July 7, 2023

    Verigene CDF Nucleic Acid Test, Part No. 30-002-22

    FDA Recall
    Open, Classified ·Luminex Corporation·Product code OZN·June 17, 2022

    Verigene Clostridium difficile Nucleic Acid Test Kit (CDF) Model Number: 20-006-022

    FDA Recall
    Open, Classified ·Luminex Corporation·Product code OCC·October 30, 2020

    VERIGENE Enteric Pathogens Nucleic Acid Test, Part No. 30-002-23

    FDA Recall
    Open, Classified ·Luminex Corporation·Product code PCH·June 17, 2022

    Verigene Enteric Pathogens Nucleic Acid Test (EP), REF 30-002-023

    FDA Recall
    Open, Classified ·Luminex Corporation·Product code PCH·June 5, 2023

    VERIGENE Clostridium difficile Nucleic Acid Test, REF 30-002-022

    FDA Recall
    Open, Classified ·Luminex Corporation·Product code OZN·June 5, 2023

    Colonoscope, Model Number PCF-H190L.

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code FDF·January 11, 2024

    Gastrointestinal videoscope-indicated for use within the upper digestive tract (including the esophagus, stomach, and duodenum). Model Numbers: GIF-1TH190, GIF-1TQ160, GIF-2T160, GIF-2TH180, GIF-H170, GIF-H180, GIF-H180J, GIF-H190, GIF-HQ190, GIF-LV1, GIF-N180, GIF-Q150, GIF-Q160Z, GIF-Q180, GIF-XP180N, GIF-XP190N, GIF-XTQ160. 510(k) Numbers: K112680, K954451, K051645, K100584, K111756, K011151, K123317.

    FDA Recall
    Open, Classified ·Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan·Product code FDF·September 25, 2023

    Colonoscope, Model Number CF-HQ190L.

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code FDF·January 11, 2024

    EVIS EXERA III Video System Center Model Number CV-190. Intended to be used with OLYMPUS camera heads, endoscopes, light sources, monitors, EndoTherapy accessories, and other ancillary equipment for endoscopic diagnosis, treatment, and video observation

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code FDF·September 14, 2023

    EVIS EXERA III Gastrointestinal Videoscope

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code FDF·October 2, 2023

    CF-HQ190L EVIS EXERA III COLONOVIDEOSCOPE

    FDA Recall
    Open, Classified ·Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan·Product code FDF·October 16, 2023

    Colonoscope, Model Number CF-HQ190I.

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code FDF·January 11, 2024

    PCF-H190DL, EVIS EXERA III COLONOVIDEOSCOPE

    FDA Recall
    Open, Classified ·Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan·Product code FDF·October 16, 2023

    GIF-HQ190, EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

    FDA Recall
    Open, Classified ·Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan·Product code FDF·October 16, 2023

    PCF-H190L, EVIS EXERA III COLONOVIDEOSCOPE

    FDA Recall
    Open, Classified ·Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan·Product code FDF·October 16, 2023

    GIF-H190, EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

    FDA Recall
    Open, Classified ·Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan·Product code FDF·October 16, 2023

    Gastroscope Family # 1-Gastroscopes without a Water Jet Channel Models: EG-2790i, EG-1690K, EG-2490K, EG-2790K, EG27-i10; Gastroscope Family # 2- Gastroscopes with a Water Jet Channel Models: EG-2990i, EG-2990K, EG-3490K, EG29-i10; Gastroscope Family # 3-Gastroscopes with Two Instrument Channels and a Water Jet Channel Models: EG-3890TK

    FDA Recall
    Open, Classified ·Pentax of America Inc·Product code FDF·July 14, 2021

    Colonoscope Family # 1-Pentax Video Colonoscopes (EC Family) with One Instrument Channel and a Water Jet Channel Models: EC-2990Li, EC-3490Li, EC-3890Li, EC-3490TLi, EC-3490LK, EC-3890LK, EC3890LZi, EC34-i10L, EC38-i10L; Colonoscope Family # 2-Pentax Video Colonoscopes with Two Instrument Channels and a Water Jet Channel Model: EC-3890TLK

    FDA Recall
    Open, Classified ·Pentax of America Inc·Product code FDF·July 14, 2021