10,000 results · 162ms · 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.

Anti-Kpa

FDA UDI
IMMUCOR, INC.·10888234000778·This reagent is used for the detection of the K...

Anti-Kpa

FDA UDI
American National Red Cross·00858400005022·Blood Grouping Reagent

EMMA™ Capnometer

FDA UDI
MASIMO CORPORATION·07350046131767·

EMMA™

FDA UDI
MASIMO CORPORATION·07350046131743·

EMMA™ Capnometer Kit

FDA UDI
MASIMO CORPORATION·07350046131514·

HU-FRIEDY

FDA UDI
HU-FRIEDY MFG. CO., LLC·10889950014643·ALLEN END-CUTTING INTRASULCULAR KNIFE

EMMA ANALYZER (KPA & MMHG); EMMA MONITOR (KPA & MMHG)

FDA 510(k)
FDA Class 2 ·Anesthesiology

EMMA ANALYZER (KPA) AND (MMHG); EMMA MONITOR (KPA) AND (MMHG)

FDA 510(k)
FDA Class 2 ·Anesthesiology

OC-Auto

FDA UDI
POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC·00816917020228·Personal Use Kit OC-Auto, for Kaiser Atlanta

BMT Medizintechnik GmbH

FDA UDI
BMT Medizintechnik GmbH·04251725224745·END-CUTTING INTRASULCULAR KNIFE

Pain Aide

FDA UDI
TENSCARE LIMITED·05033435132232·Pain Aide is a TENS device which is commonly us...

Radius PCG™

FDA UDI
MASIMO CORPORATION·07350046131996·

ARROW

FDA UDI
TELEFLEX INCORPORATED·10801902165968·FlexTip Plus(R) Epidural Catheterization Kit

ARROW

FDA UDI
TELEFLEX INCORPORATED·10801902202175·FlexTip Plus(R) Epidural Catheterization Kit

Welch Allyn, Inc.

FDA UDI
WELCH ALLYN, INC.·00732094309287·Reconditioned H12+ 12-lead digital Holter Recor...

CAPIOX®FX

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·June 25, 2025

EMMA CAPNOGRAPH, KPA

FDA Adverse Event
Malfunction ·MASIMO - 15750 ALTON PKWY·Product code CCK·February 27, 2023

EMMA CAPNOGRAPH, KPA

FDA Adverse Event
Malfunction ·MASIMO - 15750 ALTON PKWY·Product code CCK·February 27, 2023

REAGENT RED BLOOD CELLS BIOTESTCELL P3

FDA Adverse Event
Malfunction ·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code KSZ·August 25, 2015

CAPTURE-R READY-SCREEN (3)

FDA Adverse Event
Malfunction ·IMMUCOR, INC.·Product code KSZ·October 8, 2015