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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INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
126ALPHA125
In Commercial Distribution

  • B582126ALPHA1250 ()
126ALPHA125

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
126ALPHA1
In Commercial Distribution

  • B582126ALPHA10 ()
126ALPHA1

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
126ALPHA09
In Commercial Distribution

  • B582126ALPHA090 ()
126ALPHA09

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
126ALPHA08
In Commercial Distribution

  • B582126ALPHA080 ()
126ALPHA08

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
126ALPHA07
In Commercial Distribution

  • B582126ALPHA070 ()
126ALPHA07

  • Suturing unit, reusable
No Description
GEORGE TIEMANN & CO.
11030371
In Commercial Distribution

  • B582110303710 ()
11030371

  • Suturing unit, reusable
No Description
GEORGE TIEMANN & CO.
1102805SS
In Commercial Distribution

  • B5821102805SS0 ()
1102805SS

  • Suturing unit, reusable
B58211024930
GEORGE TIEMANN & CO.
B58211024930
In Commercial Distribution

  • B58211024930 ()
B58211024930

  • Suturing unit, reusable
No Description
GEORGE TIEMANN & CO.
1102403
In Commercial Distribution

  • B58211024030 ()
1102403

  • Suturing unit, reusable
No Description
GEORGE TIEMANN & CO.
1102401
In Commercial Distribution

  • B58211024010 ()
1102401

  • Suturing unit, reusable
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