SEARCH RESULTS FOR: AT(5634 results)

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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 Type Device Class Implantable

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HI-LINE XS - 04046963816315

HI-LINE XS DISP.DIAM.BURR X-CRS.II D4.0
Aesculap AG
GE556SU
In Commercial Distribution

  • 04046963816315 ()
GE556SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04046963816285

HI-LINE XS DISP.ROSEN BURR I+ D2.7MM
Aesculap AG
GE475SU
In Commercial Distribution

  • 04046963816285 ()
GE475SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04046963816278

HI-LINE XS DISP.ROSEN BURR I+ D1.8MM
Aesculap AG
GE473SU
In Commercial Distribution

  • 04046963816278 ()
GE473SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04046963816261

HI-LINE XS DISP.ROSEN BURR I+ D1.0MM
Aesculap AG
GE471SU
In Commercial Distribution

  • 04046963816261 ()
GE471SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04046963816247

HI-LINE XS DISP.ROSEN BURR I D0.6MM
Aesculap AG
GE469SU
In Commercial Distribution

  • 04046963816247 ()
GE469SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04046963816230

HI-LINE XS DISP.DIAMOND BURR I+ D2.7MM
Aesculap AG
GE465SU
Not in Commercial Distribution

  • 04046963816230 ()
GE465SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04046963816223

HI-LINE XS DISP.DIAMOND BURR I D0.8MM
Aesculap AG
GE460SU
In Commercial Distribution

  • 04046963816223 ()
GE460SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04046963816216

HI-LINE XS DISP.DIAMOND BURR I D0.6MM
Aesculap AG
GE459SU
In Commercial Distribution

  • 04046963816216 ()
GE459SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04046963816209

HI-LINE XS DISP.DIAM.BURR X-CRS.I D5.0MM
Aesculap AG
GE457SU
In Commercial Distribution

  • 04046963816209 ()
GE457SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04046963816193

HI-LINE XS DISP.DIAM.BURR X-CRS.I D4.0MM
Aesculap AG
GE456SU
In Commercial Distribution

  • 04046963816193 ()
GE456SU

  • Orthopaedic bur, single-use
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