133 results · 25ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

LIQUICHEK BLOOD GAS PLUS CO-OXIMETER CONTROL (RADIOMETER 700 SERIES) LEVELS, 1,2 AND 3, MODEL 507, 508, 509

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

TOPCUT

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

THERMO DMA FRUCTOSAMINE ASSAY, MODEL 7500-135/235

FDA 510(k)
FDA Class 2 ·Hematology

Reicodent

FDA UDI
devemed GmbH·04061644035090·Periodontal Probe # CP15 "N. Carolina" graduate...

Reicodent

FDA UDI
devemed GmbH·04061644035120·Periodontal Probe # CP11 graduated; 3-6-8-11 mm...

Reicodent

FDA UDI
devemed GmbH·04061644039623·TITAN-Periodontal Probe # CP15"North Ca" gradua...

Reicodent

FDA UDI
devemed GmbH·04061644035113·Periodontal Probe # CP11.5B (WHO) graduated; 3,...

Reicodent

FDA UDI
devemed GmbH·04061644037568·Periodontal Probe # Gold.-Fox | Williams gradua...

Reicodent

FDA UDI
devemed GmbH·04061644026142·Furcation probe "Nabers" # CQ-2N graduated; 3-6...

Reicodent

FDA UDI
devemed GmbH·04061644035083·Periodontal Probe # EX3A/CP15 graduated; 1-2......

Reicodent

FDA UDI
devemed GmbH·04061644035106·Periodontal Probe # CP12 graduated; 3-6-9-12 mm...

Reicodent

FDA UDI
devemed GmbH·04061644035137·Periodontal Probe # CP2 graduated; 2-4-6-8-10-1...

Reicodent

FDA UDI
devemed GmbH·04061644062799·Periodontal Probe # 23/CP15 graduated; 1-2...-1...

Reicodent

FDA UDI
devemed GmbH·04061644035076·Periodontal Probe # 23/CP12 graduated; 3-6-9-12...

CYSTOTOME CYSTOENTEROSTOMY NEEDLE KNIFE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code KNS·March 15, 2019

HEARTMATE II LVAS

FDA Adverse Event
Injury ·THORATEC CORP.·Product code DSQ·March 21, 2013

M SERIES

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 15, 2011

STERIS SYSTEM 1

FDA Adverse Event
Other ·STERIS CORPORATION·Product code MLR·March 24, 2008

ALINITY I STAT HIGH SENSITIVE TROPONIN-I REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code MMI·April 8, 2026

ALINITY I STAT HIGH SENSITIVE TROPONIN-I REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code MMI·April 1, 2026