27 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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g.Nautilus PRO
FDA 510(k)
FDA Class 2
·Neurology
Key Surgical K-Wires and Steinmann Pins
FDA UDI
KEY SURGICAL, INC.·00849771015109·Steinmann Pins, Single diamond, round end, 1/8-...
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704293814·
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·14026704912466·
NA
FDA UDI
KEY SURGICAL, INC.·10849771049958·Steinmann Pins, Single diamond, round end, 1/8-...
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659485198·Steinmann pin w. lanzet/round end _x000D_...
Steinmann pin w. lanzet/round end 3.2mm/229mm, 6 pcs./unit
FDA UDI
mahe medical gmbh·EMAHKM716690·Steinmann pin w. lanzet/round end
3.2mm/...
M.U.S.T. MINI POLYAXIAL SCREW
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·August 27, 2025
MUST MINI POLYAXIAL SCREW 3.5 X 12 FULL THREAD + NUT
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKG·April 6, 2018
MUST MINI POLYAXIAL SCREW 3.5 X 12 FULL THREAD + NUT
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKG·March 8, 2022
THERMODILUTION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
INTEGRA SELECTOR ULTRASONIC SURGICAL ASPIRATOR SYSTEM WITH BONE TIP
FDA 510(k)
FDA Unclassified
·Unknown
MUST MINI ROD TI 3.5 X 80MM (STERILE)
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKG·July 13, 2021
BD NANO PRO ULTRA-FINE¿ PEN NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·April 4, 2019
MUST MINI MUST MINI POLYAXIAL SCREW 3.5 X 24 FULL THREAD + NUT
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKG·July 14, 2020
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 21, 2011
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·June 15, 2013
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·October 14, 2014
PERFORMER INTRODUCER
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·April 15, 2022
PERFORMER INTRODUCER
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·September 11, 2024