339 results
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29ms
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Sources: EU EUDAMED, US FDA
Sharps Needle Destruction Device
FDA Pre-Market Approval
FDA Class 2
·THE DISINTEGRATOR INSULIN NEEDLE DESTRUCTION DEVICE
Sharps Needle Destruction Device
FDA Pre-Market Approval
FDA Class 2
·THE DISINTEGRATOR PLUS LANCE/INSULIN NEEDLE DESTRUCTON DEVICE
Sharps Needle Destruction Device
FDA Pre-Market Approval
FDA Class 2
·DISINTEGRATOR PRO NEEDLE DESTRUCTION DEVICE
Armstrong
FDA UDI
MEDTRONIC XOMED, INC.·00763000870508·VENT TUBE 1010040 5PK ARMSTRONG 7MM SIL
Armstrong
FDA UDI
MEDTRONIC XOMED, INC.·00763000038496·VENT TUBE 1010040 5PK ARMSTRONG 7MM SIL
NVJJB
FDA UDI
Nuvasive, Inc.·00887517161307·NVJJB Electrodes, Dual Wet Gel
Armstrong
FDA UDI
MEDTRONIC XOMED, INC.·00681490028134·VENT TUBE 1010040 5PK ARMSTRONG 7MM SIL
PUMA-G System™
FDA UDI
Coaptech, Inc.·00860312001504·Percutaneous Ultrasound Gastrostomy (PUG) Syste...
ENT-single-use suction tubes, angled
FDA UDI
Spiggle & Theis Medizintechnik GmbH·04250676706157·rounded tip, suction control on side
100x4....
Santis Pre Bent Rod 5.5mmx40mm
FDA UDI
Lanterna Medical Technologies GmbH·07640159550556·Santis Pre Bent Rod 5.5mmx40mm
SMALL HUDSON RATCHETING T-HANDLE
FDA UDI
Osteocentric Technologies, Inc.·00810097803848·SMALL HUDSON RATCHETING T-HANDLE
MEGA PLUS SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809763502279·Dual Locking Wrench(Short)
SANTIS™ PRE BENT ROD 5.5mm X40mm -STERILE
FDA UDI
Lanterna Medical Technologies GmbH·07640159551676·SANTIS™ PRE BENT ROD 5.5mm X40mm -STERILE
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659173279·6.5 Cancellous Bone Shaft Screw, hex, _x000D_...
6.5 Cancellous Bone Shaft Screw, hex, St.Steel, L 40/16 mm
FDA UDI
mahe medical gmbh·EMAH00100100400·6.5 Cancellous Bone Shaft Screw, hex,
St.Ste...
Integrity-SI Fusion System
FDA UDI
Lincotek Medical LLC·B57112521010040D0·10 x 40 mm Anodized SI Implant
GMA 2.0 Pedicle Screw System
FDA UDI
GRAFTON MEDICAL ALLIANCE, INC.·00810021380223·PRE-BENT ROD, ø5.5 X 40
SLEEVED FILTER
FDA 510(k)
FDA Class 2
·Anesthesiology
Implanted Fecal Incontinence Device
FDA Pre-Market Approval
FDA Class 3
·AMS ACTICON NEOSPHINCTER
Device, Thermal Ablation, Endometrial
FDA Pre-Market Approval
FDA Class 3
·HYDRO THERMABLATOR ENDOMETRIAL ABLATION SYSTEM