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 - B582105820

HANDLE, SCALPEL
GEORGE TIEMANN & CO.
10582
In Commercial Distribution

  • B582105820 ()
10582

  • Scalpel handle, reusable

N/A - B582105810

HANDLE, SCALPEL
GEORGE TIEMANN & CO.
10581
In Commercial Distribution

  • B582105810 ()
10581

  • Scalpel handle, reusable

N/A - B582105800

HANDLE, SCALPEL
GEORGE TIEMANN & CO.
10580
In Commercial Distribution

  • B582105800 ()
10580

  • Scalpel handle, reusable

N/A - B58210578960

CURETTE
GEORGE TIEMANN & CO.
1057896
In Commercial Distribution

  • B58210578960 ()
1057896

  • Dermal curette, single-use

N/A - B58210578950

CURETTE
GEORGE TIEMANN & CO.
1057895
In Commercial Distribution

  • B58210578950 ()
1057895

  • Dermal curette, single-use

N/A - B58210578940

CURETTE
GEORGE TIEMANN & CO.
1057894
In Commercial Distribution

  • B58210578940 ()
1057894

  • Dermal curette, single-use

N/A - B582105789300

CURETTE
GEORGE TIEMANN & CO.
10578930
In Commercial Distribution

  • B582105789300 ()
10578930

  • Dermal curette, single-use

N/A - B58210578930

CURETTE
GEORGE TIEMANN & CO.
1057893
In Commercial Distribution

  • B58210578930 ()
1057893

  • Dermal curette, single-use

N/A - B582105789200

CURETTE
GEORGE TIEMANN & CO.
10578920
In Commercial Distribution

  • B582105789200 ()
10578920

  • Dermal curette, single-use

N/A - B58210578920

CURETTE
GEORGE TIEMANN & CO.
1057892
In Commercial Distribution

  • B58210578920 ()
1057892

  • Dermal curette, single-use
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