32 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MPR2 logO DATALOGGER
FDA 510(k)
FDA Class 2
·Neurology
Key Surgical K-Wires and Steinmann Pins
FDA UDI
KEY SURGICAL, INC.·00849771015093·Steinmann Pins, Single diamond, round end, 7/64...
NA
FDA UDI
KEY SURGICAL, INC.·10849771049941·Steinmann Pins, Single diamond, round end, 7/64...
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·14026704912459·
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704293807·
Steinmann pin w. lanzet/round end 2.8mm/229mm, 6 pcs./unit
FDA UDI
mahe medical gmbh·EMAHKM716660·Steinmann pin w. lanzet/round end
2.8mm/...
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659485181·Steinmann pin w. lanzet/round end _x000D_...
SYNGO. PLAZA VA20A
FDA 510(k)
FDA Class 2
·Radiology
SLENDERTONE ENERVIVE, MODEL 561
FDA 510(k)
FDA Class 2
·Physical Medicine
BIZACT
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·June 18, 2019
12/14 ARTICUL 44MM M SPEC+8.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·October 14, 2014
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·June 15, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 21, 2011
BD INTIMA-II 20GAX1.16IN PRN SLM NPVC
FDA Adverse Event
Malfunction
·BD SUZHOU (MDS)·Product code FOZ·June 4, 2025
BIZACT
FDA Adverse Event
Malfunction
·COVIDIEN MFG DC BOULDER·Product code GEI·April 30, 2024
BIZACT
FDA Adverse Event
Malfunction
·COVIDIEN MFG DC BOULDER·Product code GEI·April 30, 2024
BIZACT
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·October 19, 2020
BIZACT
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·October 19, 2020
BIZACT
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·October 19, 2020
BIZACT
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·October 21, 2020