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

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ATTEST Drug Screen Cup, ATTEST Drug Screen Dip Card

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

7450 RV2 MASK

FDA UDI
HANS RUDOLPH, INC.·00874750002726·HEADGEAR LARGE V2MASK REUSEBL

SPECIAL, EMPOWR ACETABULAR, CANNULATED CUP IMPACTOR

FDA Adverse Event
Malfunction ·ENCORE MEDICAL L.P·Product code LXH·June 26, 2023

ABSORBENT PAPER POINTS

FDA UDI
DiaDent Group International·08806383511858·"An absorbent paper points is an endodontic pap...

GDC POWER SUPPLY

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - FREMONT·Product code HCG·July 20, 2010

GDC POWER SUPPLY, MODEL GDC POWER SUPPLY: 451007-4

FDA 510(k)
FDA Class 2 ·Neurology

MODIFICATION TO PROMPT L-POP

FDA 510(k)
FDA Class 2 ·Dental

ACCU-CHEK ® AVIVA PLUS TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 28, 2014

SHILEY PERCUTANEOUS

FDA Adverse Event
Injury ·COVDIEN/FORMERLY TYCO HE·Product code BTO·October 17, 2008

EON 16-CHANNEL IPG

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·August 4, 2011

LUMAX 740 VR-T DX PROMRI

FDA Adverse Event
Malfunction ·BIOTRONIK SE & CO. KG·Product code LWS·July 2, 2013

ZENITH FLEX WITH SPIRAL-Z TECHNOLOGY AAA ENDOVASCULAR GRAFT ILIAC LEG

FDA Adverse Event
Injury ·COOK INC·Product code MIH·December 19, 2017

ZENITH FLEX WITH SPIRAL-Z TECHNOLOGY AAA ENDOVASCULAR GRAFT ILIAC LEG

FDA Adverse Event
Injury ·COOK INC·Product code MIH·December 19, 2017

Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

FDA Enforcement
Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012