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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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
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
1059858
In Commercial Distribution

  • B58210598580 ()
1059858

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
1059857
In Commercial Distribution

  • B58210598570 ()
1059857

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
1059856
In Commercial Distribution

  • B58210598560 ()
1059856

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
1059855
In Commercial Distribution

  • B58210598550 ()
1059855

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
10598520
In Commercial Distribution

  • B582105985200 ()
10598520

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
10598515
In Commercial Distribution

  • B582105985150 ()
10598515

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
10598512
In Commercial Distribution

  • B582105985120 ()
10598512

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
10598510
In Commercial Distribution

  • B582105985100 ()
10598510

  • Suturing unit, reusable
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