49 results · 21ms · Sources: EU EUDAMED, US FDA

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I-STAT MODEL 200 PORTABLE CLINICAL ANALYZER

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

Creation Willi Geller

FDA UDI
KLEMA Dentalprodukte GmbH·09010782022016·In Nova Neo INN-4 red brown

Creation Willi Geller

FDA UDI
KLEMA Dentalprodukte GmbH·ECWG0011541·In Nova Neo INN-4 red brown

Health-Tec/DHP Hand Instruments

FDA UDI
Dental Health Products Inc·D77370011540·Health-Tec/DHP Plastic Filling Instrument DE 13

artVeneer life

FDA UDI
Merz Dental GmbH·D7092001154·artVeneer life lower anteriors, UCS, A4

3M QUIK TEMP TEMPORIZATION MATERIAL

FDA 510(k)
FDA Class 2 ·Dental

ELIACHAR LARYNGEAL FOAM STENT, MODEL ELL-1

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970638·

9616240-2006-00341

FDA Adverse Event
Malfunction ·Product code FII·June 14, 2006

9616240-2006-00332

FDA Adverse Event
Other ·Product code FII·June 1, 2006

PHOENIX

FDA Adverse Event
Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

9616240-2006-00339

FDA Adverse Event
Malfunction ·Product code FII·June 9, 2006

9616240-2006-00340

FDA Adverse Event
Malfunction ·Product code FII·June 9, 2006

GORE® TAG® THORACIC ENDOPROSTHESIS

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code MIH·January 6, 2016

9616240-2006-00350

FDA Adverse Event
Malfunction ·Product code FII·June 23, 2006

9616240-2006-00345

FDA Adverse Event
Malfunction ·Product code FII·June 14, 2006

MINIMED QUICK-SET

FDA Adverse Event
Injury ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·June 11, 2025

PHOENIX

FDA Adverse Event
Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

PHOENIX

FDA Adverse Event
Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

N/A

FDA UDI
Zimmer, Inc.·00889024034099·