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 - B58210578010

CURETTE
GEORGE TIEMANN & CO.
1057801
In Commercial Distribution

  • B58210578010 ()
1057801

  • Dermal curette, single-use

N/A - B58210578000

CURETTE
GEORGE TIEMANN & CO.
1057800
In Commercial Distribution

  • B58210578000 ()
1057800

  • Dermal curette, single-use

N/A - B58210577940

CURETTE
GEORGE TIEMANN & CO.
1057794
In Commercial Distribution

  • B58210577940 ()
1057794

  • Dermal curette, single-use

N/A - B58210577920

CURETTE
GEORGE TIEMANN & CO.
1057792
In Commercial Distribution

  • B58210577920 ()
1057792

  • Dermal curette, single-use

N/A - B5821057750000

No Description
GEORGE TIEMANN & CO.
10577500/0
In Commercial Distribution

  • B5821057750000 ()
10577500/0

  • Dermal curette, single-use

N/A - B58210576030

CURETTE
GEORGE TIEMANN & CO.
1057603
In Commercial Distribution

  • B58210576030 ()
1057603

  • Dermal curette, single-use

N/A - B58210576020

Curettes
GEORGE TIEMANN & CO.
1057602
In Commercial Distribution

  • B58210576020 ()
1057602

  • Dermal curette, single-use

N/A - B58210576010

Curettes
GEORGE TIEMANN & CO.
1057601
In Commercial Distribution

  • B58210576010 ()
1057601

  • Dermal curette, single-use

N/A - B58210576000

Curettes
GEORGE TIEMANN & CO.
1057600
In Commercial Distribution

  • B58210576000 ()
1057600

  • Dermal curette, single-use

N/A - B58210575760

Curettes
GEORGE TIEMANN & CO.
1057576
In Commercial Distribution

  • B58210575760 ()
1057576

  • Dermal curette, single-use
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