SEARCH RESULTS FOR: 得克萨斯A(601522 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 - B58210572430

Curettes
GEORGE TIEMANN & CO.
1057243
In Commercial Distribution

  • B58210572430 ()
1057243

  • Dermal curette, single-use

N/A - B582105724200

Curettes
GEORGE TIEMANN & CO.
10572420
In Commercial Distribution

  • B582105724200 ()
10572420

  • Dermal curette, single-use

N/A - B58210572420

Curettes
GEORGE TIEMANN & CO.
1057242
In Commercial Distribution

  • B58210572420 ()
1057242

  • Dermal curette, single-use

N/A - B58210572410

Curettes
GEORGE TIEMANN & CO.
1057241
In Commercial Distribution

  • B58210572410 ()
1057241

  • Dermal curette, single-use

N/A - B58210572400

Curettes
GEORGE TIEMANN & CO.
1057240
In Commercial Distribution

  • B58210572400 ()
1057240

  • Dermal curette, single-use

N/A - B58210572230

No Description
GEORGE TIEMANN & CO.
1057223
In Commercial Distribution

  • B58210572230 ()
1057223

  • Dermal curette, single-use

N/A - B58210572220

No Description
GEORGE TIEMANN & CO.
1057222
In Commercial Distribution

  • B58210572220 ()
1057222

  • Dermal curette, single-use

N/A - B58210572210

No Description
GEORGE TIEMANN & CO.
1057221
In Commercial Distribution

  • B58210572210 ()
1057221

  • Dermal curette, single-use

N/A - B58210572130

No Description
GEORGE TIEMANN & CO.
1057213
In Commercial Distribution

  • B58210572130 ()
1057213

  • Dermal curette, single-use

N/A - B58210572120

No Description
GEORGE TIEMANN & CO.
1057212
In Commercial Distribution

  • B58210572120 ()
1057212

  • Dermal curette, single-use
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