40 results · 22ms · 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.

AcQMap 3D Imaging and Mapping Catheter

FDA 510(k)
FDA Class 2 ·Cardiovascular

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197074964·Collin Baby Abdominal Retractor 180mm,...

THE SOLOPATH BALLOON EXPANDABLE TRANSFEMORAL INTRODUCER

FDA 510(k)
FDA Class 2 ·Cardiovascular

VARIANT II TURBO LINK HEMOGLOBIN A1C PROGRAM, AND VARIANT II TURBO LINK HEMOGLOBIN TESTING WITH MODEL, 270-2716,

FDA 510(k)
FDA Class 2 ·Hematology

DM

FDA UDI
Guilin Kevin Peter Technology Co., Ltd.·16975384335448·5 pieces

KP

FDA UDI
Guilin Kevin Peter Technology Co., Ltd.·06975384334321·

KP

FDA UDI
Guilin Kevin Peter Technology Co., Ltd.·16975384334328·5 pieces

DM

FDA UDI
Guilin Kevin Peter Technology Co., Ltd.·06975384335441·5 pieces

CURE MALE ULTRA

FDA Adverse Event
Injury ·CURE MEDICAL LLC·Product code KOD·July 13, 2018

KP

FDA UDI
Guilin Kevin Peter Technology Co., Ltd.·06975384334970·5 pieces

KP

FDA UDI
Guilin Kevin Peter Technology Co., Ltd.·16975384334977·5 pieces

ALTRUA

FDA Adverse Event
Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 21, 2011

HOMECHOICE PRO

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·June 14, 2013

ACCU-CHEK COMFORT CURVE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 15, 2008

DM

FDA UDI
Guilin Kevin Peter Technology Co., Ltd.·06975384335410·5 pieces

KP

FDA UDI
Guilin Kevin Peter Technology Co., Ltd.·06975384334314·

DM

FDA UDI
Guilin Kevin Peter Technology Co., Ltd.·16975384335424·5 pieces

DM

FDA UDI
Guilin Kevin Peter Technology Co., Ltd.·16975384335431·5 pieces

KP

FDA UDI
Guilin Kevin Peter Technology Co., Ltd.·06975384334307·

KP

FDA UDI
Guilin Kevin Peter Technology Co., Ltd.·16975384334311·5 pieces