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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 Type Device Class Implantable

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15-20 mmHg OPEN TOE KNEE-HIGH XLARGE SAND
KNIT-RITE, INC
38203
In Commercial Distribution

  • 00721734382032 ()


  • Compression/pressure sock/stocking, single-use
15-20 mmHg OPEN TOE KNEE-HIGH LARGE SAND
KNIT-RITE, INC
38202
In Commercial Distribution

  • 00721734382025 ()


  • Compression/pressure sock/stocking, single-use
15-20 mmHg OPEN TOE KNEE-HIGH MEDIUM SAND
KNIT-RITE, INC
38201
In Commercial Distribution

  • 00721734382018 ()


  • Compression/pressure sock/stocking, single-use
15-20 mmHg OPEN TOE KNEE-HIGH SMALL SAND
KNIT-RITE, INC
38200
In Commercial Distribution

  • 00721734382001 ()


  • Compression/pressure sock/stocking, single-use
15-20 mmHg OPEN TOE KNEE-HIGH XLARGE BLACK
KNIT-RITE, INC
38132
In Commercial Distribution

  • 00721734381325 ()


  • Compression/pressure sock/stocking, single-use
15-20 mmHg OPEN TOE KNEE-HIGH SMALL BRONZE
KNIT-RITE, INC
38129
In Commercial Distribution

  • 00721734381295 ()


  • Compression/pressure sock/stocking, single-use
15-20 mmHg OPEN TOE KNEE-HIGH SMALL BLACK
KNIT-RITE, INC
38128
In Commercial Distribution

  • 00721734381288 ()


  • Compression/pressure sock/stocking, single-use
15-20 mmHg OPEN TOE KNEE-HIGH LARGE BLACK
KNIT-RITE, INC
38125
In Commercial Distribution

  • 00721734381257 ()


  • Compression/pressure sock/stocking, single-use
15-20 mmHg OPEN TOE KNEE-HIGH MEDIUM BLACK
KNIT-RITE, INC
38124
In Commercial Distribution

  • 00721734381240 ()


  • Compression/pressure sock/stocking, single-use
15-20 mmHg OPEN TOE KNEE-HIGH XXLARGE BLACK
KNIT-RITE, INC
38121
In Commercial Distribution

  • 00721734381219 ()


  • Compression/pressure sock/stocking, single-use
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