SEARCH RESULTS FOR: 得克萨斯A(602335 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 - 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

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
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