SEARCH RESULTS FOR: 得克萨斯A(601548 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 - B582801435200

CURETTE
GEORGE TIEMANN & CO.
80143520
In Commercial Distribution

  • B582801435200 ()
80143520

  • Dermal curette, single-use

N/A - B58280143520

CURETTE
GEORGE TIEMANN & CO.
8014352
In Commercial Distribution

  • B58280143520 ()
8014352

  • Dermal curette, single-use

N/A - B58280143510

CURETTE
GEORGE TIEMANN & CO.
8014351
In Commercial Distribution

  • B58280143510 ()
8014351

  • Dermal curette, single-use

N/A - B58280143500

CURETTE
GEORGE TIEMANN & CO.
8014350
In Commercial Distribution

  • B58280143500 ()
8014350

  • Dermal curette, single-use

N/A - B582801431500

CURETTE
GEORGE TIEMANN & CO.
8014315/0
In Commercial Distribution

  • B582801431500 ()
8014315/0

  • Dermal curette, single-use

N/A - B582801430500

CURETTE
GEORGE TIEMANN & CO.
8014305/0
In Commercial Distribution

  • B582801430500 ()
8014305/0

  • Dermal curette, single-use

N/A - B582801430300

CURETTE
GEORGE TIEMANN & CO.
8014303/0
In Commercial Distribution

  • B582801430300 ()
8014303/0

  • Dermal curette, single-use

N/A - B582801410

CURETTE
GEORGE TIEMANN & CO.
80141
In Commercial Distribution

  • B582801410 ()
80141

  • Dermal curette, single-use

N/A - B58280140850

CURETTE
GEORGE TIEMANN & CO.
8014085
In Commercial Distribution

  • B58280140850 ()
8014085

  • Dermal curette, single-use

N/A - B58280140840

CURETTE
GEORGE TIEMANN & CO.
8014084
In Commercial Distribution

  • B58280140840 ()
8014084

  • Dermal curette, single-use
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