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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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MaXcess - 00887517145628

MaXcess MAS TLIF Blade, 110mm C-C
Nuvasive, Inc.
1628268
In Commercial Distribution

  • 00887517145628 ()


  • Surgical retraction system, reusable

MaXcess - 00887517145611

MaXcess MAS TLIF Blade, 100mm C-C
Nuvasive, Inc.
1628267
In Commercial Distribution

  • 00887517145611 ()


  • Surgical retraction system, reusable

MaXcess - 00887517145604

MaXcess MAS TLIF Blade, 90mm C-C
Nuvasive, Inc.
1628266
In Commercial Distribution

  • 00887517145604 ()


  • Surgical retraction system, reusable

MaXcess - 00887517145192

MaXcess MAS TLIF Blade, 80mm C-C
Nuvasive, Inc.
1628265
In Commercial Distribution

  • 00887517145192 ()


  • Surgical retraction system, reusable

MaXcess - 00887517145185

MaXcess MAS TLIF Blade, 70mm C-C
Nuvasive, Inc.
1628264
In Commercial Distribution

  • 00887517145185 ()


  • Surgical retraction system, reusable

MaXcess - 00887517145178

MaXcess MAS TLIF Blade, 60mm C-C
Nuvasive, Inc.
1628263
In Commercial Distribution

  • 00887517145178 ()


  • Surgical retraction system, reusable

MaXcess - 00887517145161

MaXcess MAS TLIF Blade, 50mm C-C
Nuvasive, Inc.
1628262
In Commercial Distribution

  • 00887517145161 ()


  • Surgical retraction system, reusable

MaXcess - 00887517145154

MaXcess MAS TLIF Blade, 40mm C-C
Nuvasive, Inc.
1628261
In Commercial Distribution

  • 00887517145154 ()


  • Surgical retraction system, reusable

Bausch + Lomb - 00757770440290

DIAMOND 3.0 ANG CC SHRP SIDE
Bausch & Lomb Incorporated
E0104 ACC3.0
In Commercial Distribution

  • 00757770440290 ()
E0104 ACC3.0

  • Ophthalmic knife, reusable

Bausch + Lomb - 00757770440276

DIAMOND 2.5 ANG CC SHRP SIDE
Bausch & Lomb Incorporated
E0104 ACC2.5
In Commercial Distribution

  • 00757770440276 ()
E0104 ACC2.5

  • Ophthalmic knife, reusable
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