32 results
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29ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0101100·Caddie Lid, Modular Heads, Polyaxial
InTess Lumbar Cage
FDA UDI
Kalitec Direct LLC·B07312K0101100·Distractor, Smooth Paddle, 10mm
TiWAVE L Lumbar Cage System
FDA UDI
Kalitec Direct LLC·B07323K0101100·Distractor, Smooth Paddle, Lordotic, 10mm
POWDER-FREE NITRILE EXAMINATION GLOVES, WHITE
FDA 510(k)
FDA Class 1
·General Hospital
Avitene
FDA UDI
Davol Inc.·00801741010477·Avitene Non-Woven Web, 70 mm x 70 mm x 1 mm
Santis Pre Bent Rod 5.5mmx110mm
FDA UDI
Lanterna Medical Technologies GmbH·07640159550662·Santis Pre Bent Rod 5.5mmx110mm
Minuteman
FDA UDI
Spinal Simplicity, LLC·M9432000101100·Speed Adaptor, 10mm
Integrity-SI Fusion System
FDA UDI
Lincotek Medical LLC·B57112521010110D0·10 x 110 mm Anodized SI Implant
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659173491·6.5 Cancellous Bone Shaft Screw, hex, _x000D_...
SANTIS™ PRE BENT ROD 5.5mm X110mm -STERILE
FDA UDI
Lanterna Medical Technologies GmbH·07640159551782·SANTIS™ PRE BENT ROD 5.5mm X110mm -STERILE
GMA 2.0 Pedicle Screw System
FDA UDI
GRAFTON MEDICAL ALLIANCE, INC.·00810021380315·PRE-BENT ROD, ø5.5 X 110
6.5 Cancellous Bone Shaft Screw, hex, St.Steel, L 110/16 mm
FDA UDI
mahe medical gmbh·EMAH00100101100·6.5 Cancellous Bone Shaft Screw, hex,
St.Ste...
CRYSTAL-EEG MODEL 15
FDA 510(k)
FDA Class 2
·Neurology
VALLEYLAB LIGASURE PRECISE INSTRUMENT VESSEL SEALING SYSTEM-MODEL # LS1200 & SLIGAURE GENERATOR
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BD PLASTIPAK CONCENTRIC LUER LOCK SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·June 22, 2021
BD PLASTIPAK¿ 50ML CONCENTRIC LUER LOCK SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·December 1, 2021
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013
SECURE ACUTE CARE BED 3/01
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·March 1, 2011
DISPOSABLE PET BALLOON DILATORS
FDA Adverse Event
Malfunction
·JUAREZ FACILITY·Product code KNQ·March 10, 2008
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·August 8, 2018