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 - B5821057163SS0

No Description
GEORGE TIEMANN & CO.
1057163 SS
In Commercial Distribution

  • B5821057163SS0 ()
1057163 SS

  • Dermal curette, single-use

N/A - B5821057163AS0

No Description
GEORGE TIEMANN & CO.
1057163 AS
In Commercial Distribution

  • B5821057163AS0 ()
1057163 AS

  • Dermal curette, single-use

N/A - B5821057162SS0

No Description
GEORGE TIEMANN & CO.
1057162 SS
In Commercial Distribution

  • B5821057162SS0 ()
1057162 SS

  • Dermal curette, single-use

N/A - B5821057162AS0

No Description
GEORGE TIEMANN & CO.
1057162 AS
In Commercial Distribution

  • B5821057162AS0 ()
1057162 AS

  • Dermal curette, single-use

N/A - B58210571620SS0

No Description
GEORGE TIEMANN & CO.
1057162/0 SS
In Commercial Distribution

  • B58210571620SS0 ()
1057162/0 SS

  • Dermal curette, single-use

N/A - B58210571620AS0

No Description
GEORGE TIEMANN & CO.
1057162/0 AS
In Commercial Distribution

  • B58210571620AS0 ()
1057162/0 AS

  • Dermal curette, single-use

N/A - B5821057161SS0

No Description
GEORGE TIEMANN & CO.
1057161 SS
In Commercial Distribution

  • B5821057161SS0 ()
1057161 SS

  • Dermal curette, single-use

N/A - B5821057161AS0

No Description
GEORGE TIEMANN & CO.
1057161 AS
In Commercial Distribution

  • B5821057161AS0 ()
1057161 AS

  • Dermal curette, single-use

N/A - B5821057160SS0

No Description
GEORGE TIEMANN & CO.
1057160 SS
In Commercial Distribution

  • B5821057160SS0 ()
1057160 SS

  • Dermal curette, single-use

N/A - B5821057160SB0

No Description
GEORGE TIEMANN & CO.
1057160 SB
In Commercial Distribution

  • B5821057160SB0 ()
1057160 SB

  • Dermal curette, single-use
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