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

Show Filters

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
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
1059851
In Commercial Distribution

  • B58210598510 ()
1059851

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
1059774
In Commercial Distribution

  • B58210597740 ()
1059774

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
105977375
In Commercial Distribution

  • B5821059773750 ()
105977375

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
1059773
In Commercial Distribution

  • B58210597730 ()
1059773

  • Suturing unit, reusable
No Description
GEORGE TIEMANN & CO.
105933
In Commercial Distribution

  • B5821059330 ()
105933

  • Suturing unit, reusable
No Description
GEORGE TIEMANN & CO.
105907
In Commercial Distribution

  • B5821059070 ()
105907

  • Suturing unit, reusable
INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
GEORGE TIEMANN & CO.
105900
In Commercial Distribution

  • B5821059000 ()
105900

  • Suturing unit, reusable
< 1 ... 192 193 194 195 196 ... 307 >