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 - B58210572060

Curettes
GEORGE TIEMANN & CO.
1057206
In Commercial Distribution

  • B58210572060 ()
1057206

  • Dermal curette, single-use

N/A - B58210572050

Curettes
GEORGE TIEMANN & CO.
1057205
In Commercial Distribution

  • B58210572050 ()
1057205

  • Dermal curette, single-use

N/A - B58210572040

Curettes
GEORGE TIEMANN & CO.
1057204
In Commercial Distribution

  • B58210572040 ()
1057204

  • Dermal curette, single-use

N/A - B582105720300

Curettes
GEORGE TIEMANN & CO.
10572030
In Commercial Distribution

  • B582105720300 ()
10572030

  • Dermal curette, single-use

N/A - B58210572030

Curettes
GEORGE TIEMANN & CO.
1057203
In Commercial Distribution

  • B58210572030 ()
1057203

  • Dermal curette, single-use

N/A - B582105720200

Curettes
GEORGE TIEMANN & CO.
10572020
In Commercial Distribution

  • B582105720200 ()
10572020

  • Dermal curette, single-use

N/A - B58210572020

Curettes
GEORGE TIEMANN & CO.
1057202
In Commercial Distribution

  • B58210572020 ()
1057202

  • Dermal curette, single-use

N/A - B582105720100

Curettes
GEORGE TIEMANN & CO.
1057201
In Commercial Distribution

  • B582105720100 ()
1057201

  • Dermal curette, single-use

N/A - B58210572010

Curettes
GEORGE TIEMANN & CO.
1057201
In Commercial Distribution

  • B58210572010 ()
1057201

  • Dermal curette, single-use

N/A - B58210572000

Curettes
GEORGE TIEMANN & CO.
1057200
In Commercial Distribution

  • B58210572000 ()
1057200

  • Dermal curette, single-use
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