35 results · 26ms · Sources: EU EUDAMED, US FDA

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HARMONIC FOCUS SHEARS

FDA 510(k)
FDA Unclassified ·Unknown

Thermo Scientific Pacific Hemostasis®

FDA UDI
Fisher Diagnostics·00845275000573·

HS Diam. Burr, Ø3.1x150, 80k

FDA UDI
Bien-Air Surgery SA·17630055507386·

Nitanium® Super Elastic Archwires

FDA UDI
Ortho Organizers, Inc.·00190707088156·.019x.025 Lower Nitanium® Dimple Reverse Curve ...

Portex

FDA UDI
ICU MEDICAL, INC.·15019315060304·

Portex

FDA UDI
ICU MEDICAL, INC.·15019315060281·

Portex

FDA UDI
ICU MEDICAL, INC.·15019315060298·

Portex

FDA UDI
ICU MEDICAL, INC.·15019315107153·

Portex

FDA UDI
ICU MEDICAL, INC.·15019315103018·

Portex

FDA UDI
ICU MEDICAL, INC.·15019315107146·

PASS LP

FDA Adverse Event
Injury ·MEDICREA INTL.·Product code MNI·October 14, 2011

VITA RESPONSE

FDA 510(k)
FDA Class 2 ·Dental

SYNCHRON LX SYSTEMS HIGH SENSITIVITY C-REACTIVE PROTIEN (CRPH) REAGENT

FDA 510(k)
FDA Class 2 ·Immunology

PORTEX UNIPERC PERCUTANEOUS DILATION TRACHEOSTOMY KIT

FDA Adverse Event
Malfunction ·SMITHS MEDICAL ASD, INC.·Product code BTO·February 20, 2019

PASS LP

FDA Adverse Event
Injury ·MEDICREA INTERNATIONAL·Product code MNI·November 11, 2011

PORTEX PERCUTANEOUS DILATION TRACHEOSTOMY (PDT) KIT, 8MM

FDA Adverse Event
Malfunction ·SMITHS MEDICAL CZECH REPUBLIC A. S·Product code BTO·December 30, 2024

BD PYXIS¿ ANESTHESIA STATION ES

FDA Adverse Event
Malfunction ·CAREFUSION 303, INC.·Product code BRY·May 14, 2026

ACCU-CHEK SPIRIT COMBO

FDA Adverse Event
Malfunction ·ROCHE DIABETES CARE AG·Product code LZG·May 8, 2013

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Death ·BAXTER HEATHCARE CORPORATION·Product code KDJ·September 19, 2014

CONSTELLATION WITH LASER

FDA Adverse Event
Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·May 13, 2011