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 - B58210578750

CURETTE
GEORGE TIEMANN & CO.
1057875
In Commercial Distribution

  • B58210578750 ()
1057875

  • Dermal curette, single-use

N/A - B58210578740

CURETTE
GEORGE TIEMANN & CO.
1057874
In Commercial Distribution

  • B58210578740 ()
1057874

  • Dermal curette, single-use

N/A - B58210578730

CURETTE
GEORGE TIEMANN & CO.
1057873
In Commercial Distribution

  • B58210578730 ()
1057873

  • Dermal curette, single-use

N/A - B58210578720

CURETTE
GEORGE TIEMANN & CO.
1057872
In Commercial Distribution

  • B58210578720 ()
1057872

  • Dermal curette, single-use

N/A - B58210578660

CURETTE
GEORGE TIEMANN & CO.
1057866
In Commercial Distribution

  • B58210578660 ()
1057866

  • Dermal curette, single-use

N/A - B58210578650

CURETTE
GEORGE TIEMANN & CO.
1057865
In Commercial Distribution

  • B58210578650 ()
1057865

  • Dermal curette, single-use

N/A - B58210578640

CURETTE
GEORGE TIEMANN & CO.
1057864
In Commercial Distribution

  • B58210578640 ()
1057864

  • Dermal curette, single-use

N/A - B582105786300

CURETTE
GEORGE TIEMANN & CO.
10578630
In Commercial Distribution

  • B582105786300 ()
10578630

  • Dermal curette, single-use

N/A - B58210578630

CURETTE
GEORGE TIEMANN & CO.
1057863
In Commercial Distribution

  • B58210578630 ()
1057863

  • Dermal curette, single-use

N/A - B582105786200

CURETTE
GEORGE TIEMANN & CO.
10578620
In Commercial Distribution

  • B582105786200 ()
10578620

  • Dermal curette, single-use
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