21 results · 19ms · Sources: EU EUDAMED, US FDA

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IONOMETER EF-HK AND ACCESSORIES

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

N/A

FDA UDI
Smith & Nephew, Inc.·00885556601808·SOD OBTUATOR 8 MM FOR 6901041

Welch Allyn, Inc.

FDA UDI
WELCH ALLYN, INC.·00732094233735·Welch Allyn Home Blood Pressure Monitor

Welch Allyn, Inc.

FDA UDI
WELCH ALLYN, INC.·00732094242997·WA HOME IMPLEMENTATION KIT

Welch Allyn, Inc.

FDA UDI
WELCH ALLYN, INC.·00732094079388·Welch Allyn OSZ-5 Home Blood Pressure System wi...

Welch Allyn, Inc.

FDA UDI
WELCH ALLYN, INC.·00732094246131·Welch Allyn Home Blood Pressure Monitor (1500 S...

Welch Allyn, Inc.

FDA UDI
WELCH ALLYN, INC.·06932825396010·Welch Allyn Home Blood Pressure Monitor (1500 S...

Welch Allyn, Inc.

FDA UDI
WELCH ALLYN, INC.·00732094318036·HOME CE MONITORING BLOOD PRESSURE W SBP

Welch Allyn, Inc.

FDA UDI
WELCH ALLYN, INC.·00732094323702·Welch Allyn Home Blood Pressure Monitor with Su...

Welch Allyn, Inc.

FDA UDI
WELCH ALLYN, INC.·00732094251579·TAA HOME MONITORING BLOOD PRESSURE W SBP

Welch Allyn, Inc.

FDA UDI
WELCH ALLYN, INC.·00732094317602·Welch Allyn Home Blood Pressure Monitor (1500 S...

TCP

FDA UDI
WRIGHT MEDICAL TECHNOLOGY, INC.·00840420118752·

PC

FDA UDI
Allied Medical, LLC·00026072026748·YOKE/ADPTR ASS'Y WITH "T"

CRONO S-PID 50

FDA 510(k)
FDA Class 2 ·General Hospital

COMFORT LATEX POWDERED PATIENT EXAMINATION GLOVES WITH PROTEIN LABEL CLAIM CONTAINS 200 MICROGRAMS OR LESS OF TOTAL WATE

FDA 510(k)
FDA Class 1 ·General Hospital

SYRINGE 10ML 18G 1-1/2IN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMF·June 17, 2019

ENDOSTAT 3 BIPOLAR/MONOPOLAR ELECTROSURGICAL GENERATOR

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code KNS·June 30, 2014

MINIARC SINGLE-INCISION SLING

FDA Adverse Event
Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·January 3, 2013

HARMONIC ACE 36CM W ERG HANDLE

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·November 17, 2010

STEALTHSTATION¿ S8 SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·February 28, 2024