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

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hCG Urine Test Strip, hCG Urine Test Cassette, hCG Urine Test Midstream

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772777655·LUMBAMED BASIC DORSAL STAYS M SILVER III

Integra® Jarit®

FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780182122·Integra® Jarit® Little Retractor, 7-1/2", 11.6m...

7000 CONNECTORS

FDA UDI
HANS RUDOLPH, INC.·00817136022192·CONN 28.6IDORG X28.6IDORG 7000

GERALD TISSUE FORCEPS

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896060159·GERALD TISSUE FORCEPS CROSS SERRATED TIP

Initia Total Hip System

FDA UDI
KYOCERA MEDICAL CORPORATION·04580810058027·"STDHO LINER 32-46 Size:32-46 Type:Flat, HO 32m...

DESS dental smart solutions

FDA UDI
TERRATS MEDICAL SL.·08435457202950·External Hex Universal

Initia Total Hip System

FDA UDI
KYOCERA CORPORATION·04547898307263·STDHO LINER 32-46

Minuteman

FDA UDI
Spinal Simplicity, LLC·M9432001330000·Cobb Spinal Elevator 28cm

MENICON Z

FDA 510(k)
FDA Class 2 ·Ophthalmic

MODIFICATION TO THE MAESTRO SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

BONE SCREW 6,5 H.30MM

FDA Adverse Event
Injury ·LIMA CORPORATE S.P.A.·Product code LPH·February 7, 2020

HNM MEDICAL

FDA UDI
HNM STAINLESS, LLC.·00842962160305·MINI CASE, 7"X3"X1", W/SILICONE MAT

ACCU-CHEK COMFORT CURVE TEST STRIPS

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

CAPSUREFIX NOVUS

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 10, 2011

ANIMAS INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·July 1, 2013

ENDEAVOR RX

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code NIQ·August 19, 2021

RESOLUTE INTEGRITY RX

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code NIQ·August 19, 2021

CURRENT HEALTH MONITORING SYSTEM GEN 2 (G2)

FDA Adverse Event
Death ·CURRENT HEALTH LTD·Product code MSX·September 9, 2024

ANSPACH***REF SP-4605-00***Arthroscopic Suture Anchor assembly with Suture Threader***Rx Only*** This device is intended to be used with Anspach Systems

FDA Enforcement
Class II ·Terminated·The Anspach Effort, Inc.·July 2, 2014