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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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TEC EYHANCE TOR II SMPLCTY 15.0D CYL4.50
JOHNSON & JOHNSON SURGICAL VISION, INC.
DIU450
In Commercial Distribution

  • 05050474748804 ()

  • Outer Diameter: 13 Millimeter
DIU450U150

  • Posterior-chamber intraocular lens, pseudophakic
TEC EYHANCE TOR II SMPLCTY 14.5D CYL4.50
JOHNSON & JOHNSON SURGICAL VISION, INC.
DIU450
In Commercial Distribution

  • 05050474748798 ()

  • Outer Diameter: 13 Millimeter
DIU450U145

  • Posterior-chamber intraocular lens, pseudophakic
TEC EYHANCE TOR II SMPLCTY 14.0D CYL4.50
JOHNSON & JOHNSON SURGICAL VISION, INC.
DIU450
In Commercial Distribution

  • 05050474748781 ()

  • Outer Diameter: 13 Millimeter
DIU450U140

  • Posterior-chamber intraocular lens, pseudophakic
TEC EYHANCE TOR II SMPLCTY 13.5D CYL4.50
JOHNSON & JOHNSON SURGICAL VISION, INC.
DIU450
In Commercial Distribution

  • 05050474748774 ()

  • Outer Diameter: 13 Millimeter
DIU450U135

  • Posterior-chamber intraocular lens, pseudophakic
TEC EYHANCE TOR II SMPLCTY 13.0D CYL4.50
JOHNSON & JOHNSON SURGICAL VISION, INC.
DIU450
In Commercial Distribution

  • 05050474748767 ()

  • Outer Diameter: 13 Millimeter
DIU450U130

  • Posterior-chamber intraocular lens, pseudophakic
TEC EYHANCE TOR II SMPLCTY 12.5D CYL4.50
JOHNSON & JOHNSON SURGICAL VISION, INC.
DIU450
In Commercial Distribution

  • 05050474748750 ()

  • Outer Diameter: 13 Millimeter
DIU450U125

  • Posterior-chamber intraocular lens, pseudophakic
TEC EYHANCE TOR II SMPLCTY 12.0D CYL4.50
JOHNSON & JOHNSON SURGICAL VISION, INC.
DIU450
In Commercial Distribution

  • 05050474748743 ()

  • Outer Diameter: 13 Millimeter
DIU450U120

  • Posterior-chamber intraocular lens, pseudophakic
TEC EYHANCE TOR II SMPLCTY 11.5D CYL4.50
JOHNSON & JOHNSON SURGICAL VISION, INC.
DIU450
In Commercial Distribution

  • 05050474748736 ()

  • Outer Diameter: 13 Millimeter
DIU450U115

  • Posterior-chamber intraocular lens, pseudophakic
VISCO-3 (P980044/S027) is indicated for treatment of pain in osteoarthritis (OA) of the knee in patients who have failed to respond adequately to conservative non-pharmacologic therapy and simple analgesics, e.g., acetaminophen. VISCO-3 is a sterile, viscoelastic, non-pyrogenic solution (pH of 6.8-7.8) of highly purified, high molecular weight hyaluronic acid (HA) (620 000-1 170 000 daltons). HA, which is extracted from chicken combs, is a polysaccharide containing repeating disaccharide units of glucuronic acid and N-acetylglucosamine. HA is a common constituent of the extracellular matrix of connective tissues. VISCO-3 is supplied sterile in single-use, pre-filled, disposable plastic syringes, each containing 25 mg of HA dissolved in a Phosphate Buffered Saline (PBS) solution (2.5 mL of 1.0% solution).
SEIKAGAKU CORPORATION
00-1111-001-03
In Commercial Distribution

  • 04987541301314 ()
  • 14987541301311 ()
00-1111-001-03

  • Synovial fluid supplementation medium
Gel-One is a cross-linked hyaluronate hydrogel that is indicated for the treatment of pain in osteoarthritis (OA) of the knee in patients who have failed to respond adequately to non-pharmacologic therapy, non-steroidal anti-inflammatory drugs (NSAIDs) or analgesics (e.g., acetaminophen). Gel-One is physician-administered, and is injected directly into the cavity of the knee joint. It is delivered via a single-use, pre-filled disposable glass syringe containing 3 mL of Gel-One.
SEIKAGAKU CORPORATION
00-1111-001-00
In Commercial Distribution

  • 04987541300911 ()
00-1111-001-00

  • Synovial fluid supplementation medium
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