71 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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CRYOPETTE
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Thermo Scientific Pacific Hemostasis®
FDA UDI
Fisher Diagnostics·00845275000566·
EXTRACTING FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896048348·EXTRACTING FORCEPS TUNGSTEN CARBIDE DUST TIPS #1
Pointe Scientific, Inc.
FDA UDI
HORIBA INSTRUMENTS INCORPORATED·00811727013132·T3 for the quantitative determination of the Tr...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450555774·
HS Diam. Burr, Ø1.8x150, 80k
FDA UDI
Bien-Air Surgery SA·17630055507379·
House Brand Dentistry
FDA UDI
Frontier Dental Supply Inc·00810132809538·HSB - 5.25" x 11" - Paper/Clear Film Self-Seali...
Nitanium® Super Elastic Archwires
FDA UDI
Ortho Organizers, Inc.·00190707088149·.019x.025 Upper Nitanium® Dimple Reverse Curve ...
Portex
FDA UDI
ICU MEDICAL, INC.·00351688072149·
N/A
FDA UDI
Doppkon GmbH & Co. KG·04262494463952·Micro Spoon Straight Jaw
D 2.0mm, WL 150mm
N/A
FDA UDI
Doppkon GmbH & Co. KG·04262494461644·Micro Spoon Straight Jaw
D 2.0mm, WL 150mm
Portex
FDA UDI
ICU MEDICAL, INC.·00351688072163·
Portex
FDA UDI
ICU MEDICAL, INC.·00351688072156·
RUSCH BRONCHUS BLOCKER KIT
FDA 510(k)
FDA Class 2
·Anesthesiology
ETEST GATIFLOXACIN
FDA 510(k)
FDA Class 2
·Microbiology
CAIMAN DISP. INSTR. NON ARTICUL. D:5/360MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·August 12, 2015
CAIMAN DISP. INSTR. ARTICULAT. D:12/240MM
FDA Adverse Event
Malfunction
·AESCULAP AG AND CO. KG·Product code GEI·November 11, 2014
CAIMAN DISP. INSTR. ARTICULAR D-12/240MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·May 6, 2014
CAIMAN DISP. INSTR. NON ARTICUL. D:5/360MM
FDA Adverse Event
Malfunction
·B. BRAUN SURGICAL S.A.·Product code GEI·March 21, 2014
CAIMAN DISP. INSTR. NON ARTICUL. D:5/360MM
FDA Adverse Event
Malfunction
·AESCULAP AG AND CO. KG·Product code GEI·December 12, 2014