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 - B58280140840

CURETTE
GEORGE TIEMANN & CO.
8014084
In Commercial Distribution

  • B58280140840 ()
8014084

  • Dermal curette, single-use

N/A - B58280140830

CURETTE
GEORGE TIEMANN & CO.
8014083
In Commercial Distribution

  • B58280140830 ()
8014083

  • Dermal curette, single-use

N/A - B58280140820

CURETTE
GEORGE TIEMANN & CO.
8014082
In Commercial Distribution

  • B58280140820 ()
8014082

  • Dermal curette, single-use

N/A - B58280140810

CURETTE
GEORGE TIEMANN & CO.
8014081
In Commercial Distribution

  • B58280140810 ()
8014081

  • Dermal curette, single-use

N/A - B58280140800

CURETTE
GEORGE TIEMANN & CO.
8014080
In Commercial Distribution

  • B58280140800 ()
8014080

  • Dermal curette, single-use

N/A - B58280140740

CURETTE
GEORGE TIEMANN & CO.
8014074
In Commercial Distribution

  • B58280140740 ()
8014074

  • Dermal curette, single-use

N/A - B582801407300

CURETTE
GEORGE TIEMANN & CO.
80140730
In Commercial Distribution

  • B582801407300 ()
80140730

  • Dermal curette, single-use

N/A - B58280140730

CURETTE
GEORGE TIEMANN & CO.
8014073
In Commercial Distribution

  • B58280140730 ()
8014073

  • Dermal curette, single-use

N/A - B582801407200

CURETTE
GEORGE TIEMANN & CO.
80140720
In Commercial Distribution

  • B582801407200 ()
80140720

  • Dermal curette, single-use

N/A - B58280140710

CURETTE
GEORGE TIEMANN & CO.
8014071
In Commercial Distribution

  • B58280140710 ()
8014071

  • Dermal curette, single-use
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