16 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DISP. HYPODERMIC NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704292954·
NA
FDA UDI
KEY SURGICAL, INC.·10849771049330·K-Wires, Double diamond, .054-inch (1.4mm) diam...
K-Wire w. double end lanzet point 1.37mm/102mm, 6 pcs./unit
FDA UDI
mahe medical gmbh·EMAHKM712030·K-Wire w. double end lanzet point
1.37mm...
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659484504·K-Wire w. double end lanzet point _x000D_...
Micro Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR77712031·Micro Sprint Bracket McLaugh/Benn/Trev. .018" m...
Micro Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR77712030051·Micro Sprint Bracket McLaugh/Benn/Trev. .018" m...
Micro Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR77712031001·Micro Sprint Bracket McLaugh/Benn/Trev. .018" m...
Micro Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR77712030101·Micro Sprint Bracket McLaugh/Benn/Trev. .018" m...
ABSORBENT POINTS
FDA 510(k)
FDA Class 1
·Dental
SEREINE EXTRA STRENGTH DAILY CLEANER FOR SILICONE HYDROGEL (SIHY) SOFT CONTACT LENSES
FDA 510(k)
FDA Class 2
·Ophthalmic
ARCHITECT I2000SR
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code JJE·December 29, 2022
M2A-MAGNUM PF CUP 56ODX50ID
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·April 24, 2014
XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIQ·October 3, 2012
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·February 18, 2008
1628664-2016-00211
FDA Adverse Event
Malfunction
·August 16, 2016