19 results
·
39ms
·
Sources: EU EUDAMED, US FDA
SYNTHES (U.S.A.) UNIVERSAL SPINAL PARALLEL CONNECTOR; K962608
FDA registration
EXEL INC. DBA DHL SUPPLY CHAIN (USA)·2 products·🇺🇸 United States
SYNTHES (U.S.A.) UNIVERSAL SPINAL PARALLEL CONNECTOR
FDA registration
Jabil Switzerland Manufacturing GmbH (Mezzovico)·2 products·🇨🇭 Switzerland
SYNTHES (U.S.A.) UNIVERSAL SPINAL P
FDA registration
Synthes GMBH·2 products·🇨🇭 Switzerland
SYNTHES (U.S.A.) UNIVERSAL SPINAL P
FDA registration
SYNTHES GMBH·2 products·🇨🇭 Switzerland
SYNTHES (U.S.A.) UNIVERSAL SPINAL PARALLEL CONNECTOR
FDA registration
Jabil Inc. (Brandywine)·2 products·🇺🇸 United States
SYNTHES (U.S.A.) UNIVERSAL SPINAL PARALLEL CONNECTOR
FDA registration
Jabil Switzerland Manufacturing GmbH (Hagendorf)·2 products·🇨🇭 Switzerland
SYNTHES (U.S.A.) UNIVERSAL SPINAL PARALLEL CONNECTOR
FDA 510(k)
FDA Class 2
·Orthopedic
K-Pack II 29G
FDA registration
TERUMO EUROPE N.V.·1 product·🇧🇪 Belgium
ClariFix
FDA registration
Sterigenics U.S. LLC·1 product·🇺🇸 United States
K-Pack II Needles 29G and 30G Regular Wall
FDA registration
Sterigenics Belgium Petit Rechain S.A.·1 product·🇧🇪 Belgium
29G AND 30G K-PACK II NEEDLE
FDA registration
Terumo Medical Canada, Inc.·1 product·🇨🇦 Canada
T3 CS Elecsys
FDA registration
ROCHE DIAGNOSTICS GMBH·2 products·🇩🇪 Germany
Spertilite Phototherapy Lamp
FDA registration
GLOBAL FABTECH WHEEL CHAIR (SHANGHAI) CO., LTD.·1 product·🇨🇳 China
VITEK Gram Negative Identification
FDA registration
BIOMERIEUX, INC.·1 product·🇺🇸 United States
Orthosis, Spondylolisthesis Spinal Fixation
FDA classification
FDA Class 2
·Orthosis, Spondylolisthesis Spinal Fixation
ClariFix Device
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
29G AND 30G K-PACK II NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
Unit, Cryosurgical, Accessories
FDA classification
FDA Class 2
·Unit, Cryosurgical, Accessories
Needle, Hypodermic, Single Lumen
FDA classification
FDA Class 2
·Needle, Hypodermic, Single Lumen