2,239 results · 18ms · 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.

Skin Microneedling Manual/Automated Device (Export Only)

FDA classification
FDA Not Classified ·Skin Microneedling Manual/Automated Device (Export Only)

M-QF

FDA UDI
Quality Aspirators, Inc.·00814005024400·M-QF

QEF DESIGN CORPORATION

FDA registration
QEF DESIGN CORPORATION·3 products·🇹🇼 Taiwan

GUM®

FDA UDI
SUNSTAR AMERICAS, INC.·00070942752763·PROXABRUSH REFILLS TIGHT

NA

FDA UDI
Fehling Instruments GmbH & Co. KG·04058749103908·IMA counter blade 50x35x60mm for MQC-1

NA

FDA UDI
Fehling Instruments GmbH & Co. KG·04058749103892·IMA counter blade 40x35x60mm for MQC-1

QIF-01 extended kit

FDA UDI
QUALITY IN FLOW LTD·27290016740039·QinFlow Warrior system kit - the QiF warmer is ...

QiF Blood and Fluid Warmer

FDA 510(k)
FDA Class 2 ·General Hospital

QiF Blood and Fluid Warmer

FDA 510(k)
FDA Class 2 ·General Hospital

QiF Blood and Fluid Warmer

FDA 510(k)
FDA Class 2 ·General Hospital

QiF Blood and Fluid Warmer

FDA 510(k)
FDA Class 2 ·General Hospital

Amico Diagnostic Cuff

FDA UDI
Amico Diagnostic Incorporated·00697077000523·Child 2-Piece Cuff, 1 Tube LF, Green, Female Qu...

Adcuff™

FDA UDI
AMERICAN DIAGNOSTIC CORP·00634782085155·Adapter/Connector-SPU, 2 Tube,2 Screw, F–2 Marq...

Amico Diagnostic Cuff

FDA UDI
Amico Diagnostic Incorporated·00697077000714·Adult 2-Piece Cuff, 1 Tube LF, Navy Blue, Quick...

Adcuff™

FDA UDI
AMERICAN DIAGNOSTIC CORP·00634782085124·Adapter/Connector-SPU, Y Tube,2 Screw, F - Marq...

Amico Diagnostic Cuff

FDA UDI
Amico Diagnostic Incorporated·00697077000820·Large Adult 1-Piece Cuff, 1 Tube LF, Maroon, Fe...

Adcuff™

FDA UDI
AMERICAN DIAGNOSTIC CORP·00634782085094·Adapter/Connector-SPU, 1 Tube,Bayonet, F – Marq...

QIF-01-12 extended kit

FDA UDI
QUALITY IN FLOW LTD·07290016740097·QinFlow Warrior Extreme system kit - the QiF wa...

DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·PQF·Product code MDS·July 2, 2018

AQ-Flex™ 19-C

FDA UDI
MAUNA KEA TECHNOLOGIES·03760187910772·