SEARCH RESULTS FOR: 得克萨斯A(601451 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 - 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

N/A - B58210572480

Curettes
GEORGE TIEMANN & CO.
1057248
In Commercial Distribution

  • B58210572480 ()
1057248

  • Dermal curette, single-use

N/A - B58210572460

Curettes
GEORGE TIEMANN & CO.
1057246
In Commercial Distribution

  • B58210572460 ()
1057246

  • Dermal curette, single-use

N/A - B58210572450

Curettes
GEORGE TIEMANN & CO.
1057245
In Commercial Distribution

  • B58210572450 ()
1057245

  • Dermal curette, single-use

N/A - B58210572440

Curettes
GEORGE TIEMANN & CO.
1057244
In Commercial Distribution

  • B58210572440 ()
1057244

  • Dermal curette, single-use

N/A - B582105724300

Curettes
GEORGE TIEMANN & CO.
10572430
In Commercial Distribution

  • B582105724300 ()
10572430

  • Dermal curette, single-use
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