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 - B58210575370

Curettes
GEORGE TIEMANN & CO.
1057537
In Commercial Distribution

  • B58210575370 ()
1057537

  • Dermal curette, single-use

N/A - B58210575360

Curettes
GEORGE TIEMANN & CO.
1057536
In Commercial Distribution

  • B58210575360 ()
1057536

  • Dermal curette, single-use

N/A - B58210575350

Curettes
GEORGE TIEMANN & CO.
1057535
In Commercial Distribution

  • B58210575350 ()
1057535

  • Dermal curette, single-use

N/A - B58210575340

Curettes
GEORGE TIEMANN & CO.
1057534
In Commercial Distribution

  • B58210575340 ()
1057534

  • Dermal curette, single-use

N/A - B58210575330

Curettes
GEORGE TIEMANN & CO.
1057533
In Commercial Distribution

  • B58210575330 ()
1057533

  • Dermal curette, single-use

N/A - B58210575320

Curettes
GEORGE TIEMANN & CO.
1057532
In Commercial Distribution

  • B58210575320 ()
1057532

  • Dermal curette, single-use

N/A - B58210575310

Curettes
GEORGE TIEMANN & CO.
1057531
In Commercial Distribution

  • B58210575310 ()
1057531

  • Dermal curette, single-use

N/A - B58210575260

Curettes
GEORGE TIEMANN & CO.
1057526
In Commercial Distribution

  • B58210575260 ()
1057526

  • Dermal curette, single-use

N/A - B58210575250

Curettes
GEORGE TIEMANN & CO.
1057525
In Commercial Distribution

  • B58210575250 ()
1057525

  • Dermal curette, single-use

N/A - B58210575240

Curettes
GEORGE TIEMANN & CO.
1057524
In Commercial Distribution

  • B58210575240 ()
1057524

  • Dermal curette, single-use
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