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.
1051434
In Commercial Distribution

  • B58210514340 ()
1051434

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
1051433
In Commercial Distribution

  • B58210514330 ()
1051433

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
1051431
In Commercial Distribution

  • B58210514310 ()
1051431

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
1051430
In Commercial Distribution

  • B58210514300 ()
1051430

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
1051429
In Commercial Distribution

  • B58210514290 ()
1051429

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
1051428
In Commercial Distribution

  • B58210514280 ()
1051428

  • Suturing unit, reusable
No Description
GEORGE TIEMANN & CO.
1051427
In Commercial Distribution

  • B58210514270 ()
1051427

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
1051426
In Commercial Distribution

  • B58210514260 ()
1051426

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
1051423
In Commercial Distribution

  • B58210514230 ()
1051423

  • Suturing unit, reusable
No Description
GEORGE TIEMANN & CO.
1051422
In Commercial Distribution

  • B58210514220 ()
1051422

  • Suturing unit, reusable
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