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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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H12+ - 00812345021653

Holter Recorder
MORTARA INSTRUMENT, INC.
H12PLUS-BAA-XXXXX
Not in Commercial Distribution

  • 00812345021653 ()


  • Electrocardiographic ambulatory recorder

H12+ - 00812345021646

Holter Recorder
MORTARA INSTRUMENT, INC.
H12PLUS-AAA-XXXXX
Not in Commercial Distribution

  • 00812345021646 ()


  • Electrocardiographic ambulatory recorder

N/A - 07613327568998

QBL Software License
STRYKER CORPORATION
0794111090
In Commercial Distribution

  • 07613327568998 ()
0794-111-090

  • Electronic surgical sponge-counter

SURGICOUNT - 07613327568981

+ EMR/QBL APPLICATION
STRYKER CORPORATION
0694-002-100
In Commercial Distribution

  • 07613327568981 ()
0694-002-100

  • Electronic surgical sponge-counter

SURGICOUNT - 07613327543094

+ APPLICATION
STRYKER CORPORATION
0694002090
In Commercial Distribution

  • 07613327543094 ()
0694-002-090

  • Electronic surgical sponge-counter

H3+ - 00812345027112

Holter Recorder
MORTARA INSTRUMENT, INC.
H3PLUS-BAD-XXXXX
In Commercial Distribution

  • 00812345027112 ()


  • Electrocardiographic ambulatory recorder

H3+ - 00812345027105

Holter Recorder
MORTARA INSTRUMENT, INC.
H3PLUS-BAA-XXXXX
In Commercial Distribution

  • 00812345027105 ()


  • Electrocardiographic ambulatory recorder

H12+ - 00812345027099

Holter Recorder
MORTARA INSTRUMENT, INC.
H12PLUS-AAC-XXXXX
Not in Commercial Distribution

  • 00812345027099 ()


  • Electrocardiographic ambulatory recorder

H3+ - 00812345027044

Holter Recorder
MORTARA INSTRUMENT, INC.
BURH3PR
In Commercial Distribution

  • 00812345027044 ()


  • Electrocardiographic ambulatory recorder

SURGICOUNT - 07613327545364

APPLICATION
STRYKER CORPORATION
0794001090
In Commercial Distribution

  • 07613327545364 ()
0794001090

  • Electronic surgical sponge-counter
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