SEARCH RESULTS FOR: 立陶宛U卡(www.usdtcard.org)Ms2M(19451 results)

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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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Arthrex® - 00888867186521

JumpStart, 8" X 8", Single Layer
ARTHREX, INC.
R0808-02
In Commercial Distribution

  • 00888867186521 ()
  • M150R0808020 ()
  • 10888867186528 ()
R0808-02

  • Exudate-absorbent dressing, non-gel, antimicrobial

Arthrex® - 00888867186514

JUMPSTART, 8" X 8", SINGLE LAYER
ARTHREX, INC.
R0808-01
Not in Commercial Distribution

  • 00888867186514 ()
  • M150R0808010 ()
R0808-01

  • Exudate-absorbent dressing, non-gel, antimicrobial

Arthrex® - 00888867186507

JUMPSTART, 4" X 4", SINGLE LAYER
ARTHREX, INC.
R0404-10
In Commercial Distribution

  • 00888867186507 ()
  • M150R0404100 ()
  • 10888867186504 ()
R0404-10

  • Exudate-absorbent dressing, non-gel, antimicrobial

Arthrex® - 00888867186491

JUMPSTART, 3" X 3", SINGLE LAYER
ARTHREX, INC.
R0303-10
In Commercial Distribution

  • 00888867186491 ()
  • M150R0303100 ()
  • 10888867186498 ()
R0303-10

  • Exudate-absorbent dressing, non-gel, antimicrobial

Arthrex® - 00888867186484

JUMPSTART, 2" X 5", SINGLE LAYER
ARTHREX, INC.
R0205-10
In Commercial Distribution

  • 00888867186484 ()
  • M150R0205100 ()
  • 10888867186481 ()
R0205-10

  • Exudate-absorbent dressing, non-gel, antimicrobial

Arthrex® - 00888867186477

JUMPSTART, 2" X 2", SINGLE LAYER
ARTHREX, INC.
R0202-10
In Commercial Distribution

  • 00888867186477 ()
  • M150R0202100 ()
  • 10888867186474 ()
R0202-10

  • Exudate-absorbent dressing, non-gel, antimicrobial

Arthrex® - 00888867186453

JUMPSTART, 6" X 12.6", HELIX COMP. LAYER
ARTHREX, INC.
HR0612-05
In Commercial Distribution

  • 00888867186453 ()
  • M150HR0612050 ()
  • 10888867186450 ()
HR0612-05

  • Exudate-absorbent dressing, non-gel, antimicrobial

KGTI™ Kinetik Great Toe Implant System - 10381780065487

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

KGTI™ Kinetik Great Toe Implant System - 10381780065470

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.
012014
Not in Commercial Distribution

  • M2480120141 ()
  • 10381780065470 ()

  • .776 in dia x .662 in L; Size 2
012014

  • Partial metatarsophalangeal joint prosthesis

KGTI™ Kinetik Great Toe Implant System - 10381780065463

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.
012012
Not in Commercial Distribution

  • M2480120121 ()
  • 10381780065463 ()

  • .734 in dia x .662 in L; Size 1
012012

  • Partial metatarsophalangeal joint prosthesis
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