SEARCH RESULTS FOR: ("hf acquisition co")(39637 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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N/A - B58210578910

CURETTE
GEORGE TIEMANN & CO.
1057891
In Commercial Distribution

  • B58210578910 ()
1057891

  • Dermal curette, single-use

N/A - B58210578900

CURETTE
GEORGE TIEMANN & CO.
1057890
In Commercial Distribution

  • B58210578900 ()
1057890

  • Dermal curette, single-use

N/A - B58210578830

CURETTE
GEORGE TIEMANN & CO.
1057883
In Commercial Distribution

  • B58210578830 ()
1057883

  • Dermal curette, single-use

N/A - B582105788200

CURETTE
GEORGE TIEMANN & CO.
10578820
In Commercial Distribution

  • B582105788200 ()
10578820

  • Dermal curette, single-use

N/A - B58210578820

CURETTE
GEORGE TIEMANN & CO.
1057882
In Commercial Distribution

  • B58210578820 ()
1057882

  • Dermal curette, single-use

N/A - B58210578810

CURETTE
GEORGE TIEMANN & CO.
1057881
In Commercial Distribution

  • B58210578810 ()
1057881

  • Dermal curette, single-use

N/A - B58210578800

CURETTE
GEORGE TIEMANN & CO.
1057880
In Commercial Distribution

  • B58210578800 ()
1057880

  • Dermal curette, single-use

N/A - B58210578760

CURETTE
GEORGE TIEMANN & CO.
1057876
In Commercial Distribution

  • B58210578760 ()
1057876

  • Dermal curette, single-use

N/A - B58210578750

CURETTE
GEORGE TIEMANN & CO.
1057875
In Commercial Distribution

  • B58210578750 ()
1057875

  • Dermal curette, single-use

N/A - B58210578740

CURETTE
GEORGE TIEMANN & CO.
1057874
In Commercial Distribution

  • B58210578740 ()
1057874

  • Dermal curette, single-use
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