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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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No Description
PROTEK MEDICAL PRODUCTS, INC.
5445
In Commercial Distribution

  • 10841912101464 ()
  • 00841912101467 ()
5445

  • Needle guide, single-use
No Description
PROTEK MEDICAL PRODUCTS, INC.
5431
In Commercial Distribution

  • 10841912101440 ()
  • 00841912101443 ()
5431

  • Needle guide, single-use
No Description
PROTEK MEDICAL PRODUCTS, INC.
5430
In Commercial Distribution

  • 10841912101433 ()
  • 00841912101436 ()
5430

  • Needle guide, single-use
No Description
PROTEK MEDICAL PRODUCTS, INC.
5406
In Commercial Distribution

  • 10841912101389 ()
  • 00841912101382 ()
5406

  • Needle guide, single-use
No Description
PROTEK MEDICAL PRODUCTS, INC.
5405
In Commercial Distribution

  • 10841912101372 ()
  • 00841912101375 ()
5405

  • Needle guide, single-use
No Description
PROTEK MEDICAL PRODUCTS, INC.
5404
In Commercial Distribution

  • 10841912101365 ()
  • 00841912101368 ()
5404

  • Needle guide, single-use
No Description
PROTEK MEDICAL PRODUCTS, INC.
5403
In Commercial Distribution

  • 10841912101358 ()
  • 00841912101351 ()
5403

  • Needle guide, single-use
No Description
PROTEK MEDICAL PRODUCTS, INC.
5402
In Commercial Distribution

  • 10841912101341 ()
  • 00841912101344 ()
5402

  • Needle guide, single-use
No Description
PROTEK MEDICAL PRODUCTS, INC.
5401
In Commercial Distribution

  • 10841912101334 ()
  • 00841912101337 ()
5401

  • Needle guide, single-use
No Description
PROTEK MEDICAL PRODUCTS, INC.
5325
In Commercial Distribution

  • 10841912101327 ()
  • 00841912101320 ()
5325

  • Needle guide, single-use
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