27 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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GSU HANDPIECE ADAPTER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
TARGETING ARM, LEFT
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665032192·
Greenwald Surgical Company, Inc.
FDA UDI
GRACE MANUFACTURING, INC.·10801334010058·TONSIL ELECTRODE
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955939006·Percutaneous Transluminal Angioplasty Balloon C...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955936661·Percutaneous Transluminal Angioplasty Balloon C...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955937835·Percutaneous Transluminal Angioplasty Balloon C...
MetaSystems Probes
FDA UDI
MetaSystems Probes GmbH·04251315817807·CL 2p23 ALK BA, Break Apart Probe
FROSTED GLASS SLIDES
FDA 510(k)
FDA Class 1
·Pathology
SL 803, SL 804, SL 807, SL 809, SL 506, SL 501, SL 805 AND SL 801 MECHANICAL WHEELCHAIRS
FDA 510(k)
FDA Class 1
·Physical Medicine
PositionPRO
FDA UDI
STRYKER CORPORATION·07613327277685·
Pulmoguard
FDA UDI
S D I DIAGNOSTICS INC·B279S297920100·
Widex
FDA UDI
Widex A/S·05706069370294·Widex mind220 M2-9 BTE (Jet black ) Telecoil, R...
Widex
FDA UDI
Widex A/S·05706069370300·Widex mind220 M2-9 BTE (Cappuccino brown ) Tele...
Widex
FDA UDI
Widex A/S·05706069370324·Widex mind220 M2-9 BTE (Titan grey ) Telecoil, ...
Widex
FDA UDI
Widex A/S·05706069370317·Widex mind220 M2-9 BTE (Winter silver ) Telecoi...
Widex
FDA UDI
Widex A/S·05706069370287·Widex mind220 M2-9 BTE (Warm beige ) Telecoil, ...
Widex
FDA UDI
Widex A/S·05706069370331·Widex mind220 M2-9 BTE (Tan silk ) Telecoil, RC...
PINNACLE MTL INS NEUT36IDX54OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·January 17, 2013
DUR DYNAMIC LOCK RING 56 OR 68
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·December 3, 2010
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 8, 2014