30 results · 22ms · Sources: EU EUDAMED, US FDA

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MiniMed Connect kit, MiniMed Connect uploader, MiniMed Connect app, CareLink Connect (CareLink Personal)

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·24026704283143·DEAVER RETRACTOR HOLLOW 2 1/2" X 14 1/2"

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587T1512360·15mm TLIF Implant 12mm Wide 36mm Length

ProLift

FDA UDI
Life Spine, Inc.·00190837117412·

Pro Lift Instruments

FDA UDI
Life Spine, Inc.·00190837031190·

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587T15123670·15mm TLIF Implant 12mm Wide 36mm Length 7 Degrees

NA

FDA UDI
Biedermann Motech GmbH & Co. KG·04250869607827·TELIX K Ti Cage 12x36mm 5°

VOLUSON E6/E8/E8 EXPERT DIAGNOSTIC ULTRASOUND SYSTEM MODEL: H48681BD/ H48681BX/ H48681BM

FDA 510(k)
FDA Class 2 ·Radiology

RESORB-X SF

FDA 510(k)
FDA Class 2 ·Dental

BD VACUTAINER® LH (LITHIUM HEPARIN) 68 I.U. PLUS BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 14, 2021

11CM ANGLE ATTACHMENT

FDA Adverse Event
Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·October 8, 2014

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013

STANDARD INSERT

FDA Adverse Event
Injury ·DEPUY-CORK, A DIVISION OF DEPUY ORTHOPAEDICS·Product code KWA·June 30, 2011

INTROCAN SAFETY® 3

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·November 14, 2025

INTROCAN SAFETY® 3

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·November 12, 2025

UNIVERSA FIRM URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·June 25, 2019

UNIVERSA FIRM URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·June 25, 2019

UNIVERSA FIRM URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·June 26, 2019

INTROCAN SAFETY® 3

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FOZ·February 20, 2026

UNIVERSA FIRM URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·December 31, 2019