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