32 results · 27ms · Sources: EU EUDAMED, US FDA

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S30/S40 Digital Color Doppler Ultraound System

FDA 510(k)
FDA Class 2 ·Radiology

N/A

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00681490542418·HANDLE 9150045 TREPHINE DRIVER

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526768499·GENUMEDI PSS GREEN V

TMA - Archwire

FDA UDI
ORMCO CORPORATION·00889989029598·TMA REV.CURVE/LOOPS 019X025 38MM PK/5

RUSCH

FDA UDI
TELEFLEX INCORPORATED·04026704319695·SLICK SET UNCUFFED STERILE

Assay,Enzyme Linked Immunosorbent,Parvovirus B19 Igg

FDA Pre-Market Approval
FDA Class 3 ·ZEUS ELISA PARVOVIRUS B19 IGG TEST SYSTEM

Ophthalmic Speculum

FDA UDI
KATENA PRODUCTS, INC.·00841668100134·KRATZ-BARRAQUER SPECULUM LEFT EYE

Mariner MCT

FDA UDI
Seaspine Orthopedics Corporation·10889987167930·CORTICAL SHANK, Cannulated, 5.0 X 45

OCTO

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

INTERFUSE DA INVERTEBRAL BODY FUSION DEVICE

FDA 510(k)
FDA Class 2 ·Orthopedic

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351109454·LAP-Instrument, Ø5mm, l=450mm, flushp. Graspi...

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351115790·LAP-Instrument, Ø5mm, l=450mm, detach. Graspi...

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351105401·LAP-Instrument, Ø5mm, l=450mm, detach. Graspi...

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351118081·LAP-Insert only, Ø5mm, l=450mm Graspi...

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351113185·LAP-Instrument, Ø5mm, l=450mm, detach. Graspi...

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351111310·LAP-Instrument, Ø5mm, l=450mm, detach. Graspi...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197057691·Pelkmann Swab Forceps 250mm,...

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351103247·LAP-Instrument, Ø5mm, l=450mm, flushp. Graspi...

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 7, 2014

AUTOPULSE NIMH BATTERY

FDA Adverse Event
Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·May 20, 2013