29 results · 23ms · 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.

VAXCEL PICC WITH PASV VALVE TECHNOLOGY

FDA 510(k)
FDA Class 2 ·General Hospital

PureBliss

FDA UDI
PURELIFE, LLC·D79010217041·PureBliss Latex Powder-Free, Large, PureLife do...

Vital Signs™

FDA UDI
AirLife Finland Oy·10889483576328·Vital Signs™ direct connect temperature cable f...

Vital Signs™

FDA UDI
AirLife Finland Oy·10190752113664·Direct Connect Temperature Cable for GE Monitor...

Vital Signs™

FDA UDI
AirLife Finland Oy·10190752179318·Direct Connect Temperature Cable for GE Monitor...

Vital Signs

FDA UDI
Carefusion Finland 320 Oy·10885403288111·Direct Connect Temperature Cable for GE Monitor...

Reicodent

FDA UDI
devemed GmbH·04061644051045·Filling Instrument, cylindrical 2.0 / 2.5 mm, s...

Reicodent

FDA UDI
devemed GmbH·04061644050673·Filling Instrument, cylindrical 0.8 / 1.0 mm, s...

Reicodent

FDA UDI
devemed GmbH·04061644050697·Filling Instrument, cylindrical 1.6 / 2.0 mm, s...

Reicodent

FDA UDI
devemed GmbH·04061644050680·Filling Instrument, cylindrical 1.2 / 1.6 mm, s...

NPAC EAR THERMOMETER MODEL TD 402

FDA 510(k)
FDA Class 2 ·General Hospital

ATHOS

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

Reicodent

FDA UDI
devemed GmbH·04061644035335·Filling Instrument, cylindrical 1.6 / 2.0 mm, s...

Reicodent

FDA UDI
devemed GmbH·04061644035342·Filling Instrument, cylindrical 2.0 / 2.5 mm, s...

Reicodent

FDA UDI
devemed GmbH·04061644035328·Filling Instrument, cylindrical 1.2 / 1.6 mm, s...

Reicodent

FDA UDI
devemed GmbH·04061644027316·Filling Instrument, cylindrical 1.2 / 1.6 mm, s...

Reicodent

FDA UDI
devemed GmbH·04061644035311·Filling Instrument, cylindrical 0.8 / 1.0 mm, s...

Reicodent

FDA UDI
devemed GmbH·04061644031672·Filling Instrument, cylindrical 0.8 / 1.0 mm, s...

FREESTYLE FLASH

FDA Adverse Event
Injury ·Product code NBW·February 25, 2011

TOTAL ASR FEM IMP SIZE 46

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·March 1, 2018