25 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OVision Imaging System
FDA 510(k)
FDA Class 2
·Radiology
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772777679·LUMBAMED BASIC DORSAL STAYS M SILVER V
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772777624·LUMBAMED BASIC DORSAL STAYS WM SILVER V
7020 CONNECTORS
FDA UDI
HANS RUDOLPH, INC.·00817136022284·CONN 22ID X 22ID 7020 SERIES
Sportex
FDA UDI
Diversified Products, Inc.·00842894170496·
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112601·BARRON CORNEAL PUNCH 7.25MM
BALANCE MICROPLASTY BROACH
FDA UDI
Biomet Orthopedics, LLC·00880304459229·
ACRA-CUT
FDA UDI
ACRA-CUT INC·00810607002754·Disposable Cranial Perforator
Autolith Touch
FDA UDI
NORTHGATE TECHNOLOGIES INC.·00817183020493·Lithotripter, Biliary, BSC
DATEX-OHMEDA TEC 6 PLUS ANESTHESIA VAPORIZER, DATEX-OHMEDA TEC 6 PLUS NAD VARIANT ANESTHESIA
FDA 510(k)
FDA Class 2
·Anesthesiology
WORKING ELEMENT, RESECTION BUTTON ELECTRODE FOR PLASMA VAPORIZATON, HF-RESECTION ELECTRODE LOOPS AND BANDS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
AUTOLITH TOUCH
FDA Adverse Event
Malfunction
·NORTHGATE TECHNOLOGIES, INC·Product code FFK·September 25, 2021
PHYSICA TT
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code MBH·December 21, 2023
Disposable Cranial Perforator
FDA UDI
ACRA-CUT INC·00810607000088·Cranial Perforator
PLATE MUELLER HINTON II AGAR
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code JTZ·October 26, 2022
ANIMAS INSULIN CARTRIDGE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·April 29, 2016
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FKX·October 24, 2014
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 11, 2011
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code OYC·July 1, 2013
i-STAT CG8+ cartridge. List Number: 03P88-25. 510(k) numbers: K894914, K940918, K223710, K230275, K230285, K230300
FDA Recall
Open, Classified
·Abbott Point Of Care Inc.·Product code CHL·August 21, 2025