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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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Resolve Matrix™ 6 cm x 8 cm
DSM BIOMEDICAL, INC.
30052-29
In Commercial Distribution

  • 00812337020572 ()

  • Length: 6 Centimeter
  • Width: 8 Centimeter
RMAD68

  • Animal-derived wound matrix dressing
Resolve Matrix™ 4 cm x 5 cm
DSM BIOMEDICAL, INC.
30052-28
In Commercial Distribution

  • 00812337020565 ()

  • Length: 4 Centimeter
  • Width: 5 Centimeter
RMAD45

  • Animal-derived wound matrix dressing
Resolve Matrix™ 2 cm x 4 cm
DSM BIOMEDICAL, INC.
30052-27
In Commercial Distribution

  • 00812337020558 ()

  • Length: 2 Centimeter
  • Width: 4 Centimeter
RMAD24

  • Animal-derived wound matrix dressing
Resolve Matrix™ 2 cm x 2 cm
DSM BIOMEDICAL, INC.
30052-26
In Commercial Distribution

  • 00812337020541 ()

  • Length: 2 Centimeter
  • Width: 2 Centimeter
RMAD22

  • Animal-derived wound matrix dressing
No Description
DSM BIOMEDICAL, INC.
30052-25
In Commercial Distribution

  • 00812337020534 ()

  • Length: 10 Centimeter
  • Width: 15 Centimeter
RMAD1015

  • Animal-derived wound matrix dressing
No Description
DSM BIOMEDICAL, INC.
30052-24
In Commercial Distribution

  • 00812337020503 ()

  • Length: 10 Centimeter
  • Width: 10 Centimeter
RMAD1010

  • Animal-derived wound matrix dressing
No Description
DSM BIOMEDICAL, INC.
30052-23
In Commercial Distribution

  • 00812337020497 ()

  • Length: 6 Centimeter
  • Width: 12 Centimeter
RMAD612

  • Animal-derived wound matrix dressing
No Description
DSM BIOMEDICAL, INC.
30052-22
In Commercial Distribution

  • 00812337020480 ()

  • Length: 5 Centimeter
  • Width: 5 Centimeter
RMAD55

  • Animal-derived wound matrix dressing
No Description
DSM BIOMEDICAL, INC.
30052-21
In Commercial Distribution

  • 00812337020473 ()

  • Length: 3.5 Centimeter
  • Width: 3.5 Centimeter
RMAD3535

  • Animal-derived wound matrix dressing
The KGTI phalangeal component is fixed by means of a stem, which is inserted into the medullary canal of the phalanx. The implant is indicated for use in patients with osteoarthritis of the first metatarsophalangeal joint, trauma involving the first metatarsophalangeal joint, hallux rigidus with degenerative joint disease or arthritis.
Ascension Orthopedics, Inc.
012016
Not in Commercial Distribution

  • M2480120161 ()
  • 10381780065487 ()

  • .816 in dia x .662 in L; Size 3
012016

  • Partial metatarsophalangeal joint prosthesis
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