SEARCH RESULTS FOR: ("hf acquisition co")(39639 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 - B58210578600

CURETTE
GEORGE TIEMANN & CO.
1057860
In Commercial Distribution

  • B58210578600 ()
1057860

  • Dermal curette, single-use

N/A - B58210578550

CURETTE
GEORGE TIEMANN & CO.
1057855
In Commercial Distribution

  • B58210578550 ()
1057855

  • Dermal curette, single-use

N/A - B58210578540

CURETTE
GEORGE TIEMANN & CO.
1057854
In Commercial Distribution

  • B58210578540 ()
1057854

  • Dermal curette, single-use

N/A - B582105785300

CURETTE
GEORGE TIEMANN & CO.
10578530
In Commercial Distribution

  • B582105785300 ()
10578530

  • Dermal curette, single-use

N/A - B58210578530

CURETTE
GEORGE TIEMANN & CO.
1057853
In Commercial Distribution

  • B58210578530 ()
1057853

  • Dermal curette, single-use

N/A - B582105785200

CURETTE
GEORGE TIEMANN & CO.
10578520
In Commercial Distribution

  • B582105785200 ()
10578520

  • Dermal curette, single-use

N/A - B58210578520

CURETTE
GEORGE TIEMANN & CO.
1057852
In Commercial Distribution

  • B58210578520 ()
1057852

  • Dermal curette, single-use

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
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