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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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MAXFRAME - 10886982338778

MAXFRAME AUTOSTRUT(TM) AUTOMATED HEXAPOD ACCESSORIES
SYNTHES (U.S.A.) LP
1100022-01
In Commercial Distribution

  • 10886982338778 ()
110002201

  • External orthopaedic fixation system, single-use

MAXFRAME - 10886982338600

MAXFRAME AUTOSTRUT(TM) AUTOMATED HEXAPOD CTRL SYS KIT
SYNTHES (U.S.A.) LP
1100007-01
In Commercial Distribution

  • 10886982338600 ()
110000701

  • External orthopaedic fixation system, single-use

MAXFRAME - 10886982338594

MAXFRAME AUTOSTRUT(TM) HEXAPOD STRUT - SHORT
SYNTHES (U.S.A.) LP
1100012-01
In Commercial Distribution

  • 10886982338594 ()
110001201

  • External orthopaedic fixation system, single-use

MAXFRAME - 10886982338587

MAXFRAME AUTOSTRUT(TM) HEXAPOD STRUT - MEDIUM
SYNTHES (U.S.A.) LP
1100010-01
In Commercial Distribution

  • 10886982338587 ()
110001001

  • External orthopaedic fixation system, single-use

MAXFRAME - 10886982338570

MAXFRAME AUTOSTRUT(TM) HEXAPOD STRUT - LONG
SYNTHES (U.S.A.) LP
1100011-01
In Commercial Distribution

  • 10886982338570 ()
110001101

  • External orthopaedic fixation system, single-use

Acute QC Strut and Components - 00885556807088

ACUTE QC STRUT LONG
Smith & Nephew, Inc.
71935869
In Commercial Distribution

  • 00885556807088 ()
71935869

  • External orthopaedic fixation system, single-use

Acute QC Strut and Components - 00885556807071

ACUTE QC STRUT MEDIUM
Smith & Nephew, Inc.
71935868
In Commercial Distribution

  • 00885556807071 ()
71935868

  • External orthopaedic fixation system, single-use

Acute QC Strut and Components - 00885556807064

ACUTE QC STRUT SHORT
Smith & Nephew, Inc.
71935867
In Commercial Distribution

  • 00885556807064 ()
71935867

  • External orthopaedic fixation system, single-use

Acute QC Strut and Components - 00885556807057

ACUTE QC STRUT XSHORT
Smith & Nephew, Inc.
71935866
In Commercial Distribution

  • 00885556807057 ()
71935866

  • External orthopaedic fixation system, single-use

True Lok System - 18054242512639

DOUBLE ROW FOOTPLATE, 220MM, TL-HEX STERILE
ORTHOFIX SRL
1
In Commercial Distribution

  • 18054242512639 ()

  • Internal diameter 220 mm
99-56-22100

  • External orthopaedic fixation system, single-use
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