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 - B58210575230

Curettes
GEORGE TIEMANN & CO.
1057523
In Commercial Distribution

  • B58210575230 ()
1057523

  • Dermal curette, single-use

N/A - B58210575220

Curettes
GEORGE TIEMANN & CO.
1057522
In Commercial Distribution

  • B58210575220 ()
1057522

  • Dermal curette, single-use

N/A - B58210575210

Curettes
GEORGE TIEMANN & CO.
1057521
In Commercial Distribution

  • B58210575210 ()
1057521

  • Dermal curette, single-use

N/A - B58210575030

Curettes
GEORGE TIEMANN & CO.
1057503
In Commercial Distribution

  • B58210575030 ()
1057503

  • Dermal curette, single-use

N/A - B58210575020

Curettes
GEORGE TIEMANN & CO.
1057502
In Commercial Distribution

  • B58210575020 ()
1057502

  • Dermal curette, single-use

N/A - B58210575010

Curettes
GEORGE TIEMANN & CO.
1057501
In Commercial Distribution

  • B58210575010 ()
1057501

  • Dermal curette, single-use

N/A - B5821057470

Curettes
GEORGE TIEMANN & CO.
105747
In Commercial Distribution

  • B5821057470 ()
105747

  • Dermal curette, single-use

N/A - B5821057258100

Curettes
GEORGE TIEMANN & CO.
105725810
In Commercial Distribution

  • B5821057258100 ()
105725810

  • Dermal curette, single-use

N/A - B582105725680

Curettes
GEORGE TIEMANN & CO.
10572568
In Commercial Distribution

  • B582105725680 ()
10572568

  • Dermal curette, single-use

N/A - B58210572510120

Curettes
GEORGE TIEMANN & CO.
1057251012
In Commercial Distribution

  • B58210572510120 ()
1057251012

  • Dermal curette, single-use
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