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 - B58210578510

CURETTE
GEORGE TIEMANN & CO.
1057851
In Commercial Distribution

  • B58210578510 ()
1057851

  • Dermal curette, single-use

N/A - B58210578500

CURETTE
GEORGE TIEMANN & CO.
1057850
In Commercial Distribution

  • B58210578500 ()
1057850

  • Dermal curette, single-use

N/A - B58210578260

CURETTE
GEORGE TIEMANN & CO.
1057826
In Commercial Distribution

  • B58210578260 ()
1057826

  • Dermal curette, single-use

N/A - B58210578240

CURETTE
GEORGE TIEMANN & CO.
1057824
In Commercial Distribution

  • B58210578240 ()
1057824

  • Dermal curette, single-use

N/A - B58210578220

CURETTE
GEORGE TIEMANN & CO.
1057822
In Commercial Distribution

  • B58210578220 ()
1057822

  • Dermal curette, single-use

N/A - B58210578040

CURETTE
GEORGE TIEMANN & CO.
1057804
In Commercial Distribution

  • B58210578040 ()
1057804

  • Dermal curette, single-use

N/A - B582105780300

CURETTE
GEORGE TIEMANN & CO.
10578030
In Commercial Distribution

  • B582105780300 ()
10578030

  • Dermal curette, single-use

N/A - B58210578030

CURETTE
GEORGE TIEMANN & CO.
1057803
In Commercial Distribution

  • B58210578030 ()
1057803

  • Dermal curette, single-use

N/A - B582105780200

CURETTE
GEORGE TIEMANN & CO.
10578020
In Commercial Distribution

  • B582105780200 ()
10578020

  • Dermal curette, single-use

N/A - B58210578020

CURETTE
GEORGE TIEMANN & CO.
1057802
In Commercial Distribution

  • B58210578020 ()
1057802

  • Dermal curette, single-use
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