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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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Malosa Core SMILE Pack 1 (20/SP)
Beaver-Visitec International, Inc.
MMK884
In Commercial Distribution

  • 05055186236953 ()
  • 35055186236954 ()
MMK844

  • Ophthalmic surgical procedure kit, non-medicated, single-use
Malosa Core Suface Treatment Pack (20/SP)
Beaver-Visitec International, Inc.
MMK110/3
In Commercial Distribution

  • 05055186236069 ()
  • 35055186236060 ()
MMK110/3

  • Ophthalmic surgical procedure kit, non-medicated, single-use
Malosa Core LASIK Pack 2 (20/SP)
Beaver-Visitec International, Inc.
MMK100/2
In Commercial Distribution

  • 05055186236052 ()
  • 35055186236053 ()
MMK100/2

  • Ophthalmic surgical procedure kit, non-medicated, single-use
Easy@Home Ketone Test Strips (20 Pack)
EASY HEALTHCARE CORPORATION
EZR-101
In Commercial Distribution

  • 00810038631431 ()
  • 30810038631432 ()
EZR-101-20(P)

  • Urine ketone IVD, kit, rapid colorimetric, clinical
Therma-Kor Endo Obturator 25mm #20 (6/PK)
XLENT GLOBAL INC
TK-46062520
In Commercial Distribution

  • 00810135270014 ()
TK-46062520

  • Warm-bonded endodontic obturation system obturator
Trial, 30 x 38mm, 20° Lordotic, 19mm
CAMBER SPINE TECHNOLOGIES, LLC
SPA-102-041
In Commercial Distribution

  • B030SPA1020410 ()


  • Spinal implant trial
Trial, 30 x 38mm, 20° Lordotic, 17mm
CAMBER SPINE TECHNOLOGIES, LLC
SPA-102-040
In Commercial Distribution

  • B030SPA1020400 ()


  • Spinal implant trial
Trial, 30 x 38mm, 20° Lordotic, 15mm
CAMBER SPINE TECHNOLOGIES, LLC
SPA-102-039
In Commercial Distribution

  • B030SPA1020390 ()


  • Spinal implant trial
Trial, 30 x 38mm, 20° Lordotic, 13mm
CAMBER SPINE TECHNOLOGIES, LLC
SPA-102-038
In Commercial Distribution

  • B030SPA1020380 ()


  • Spinal implant trial
Trial, 26 x 32mm, 20° Lordotic, 15mm
CAMBER SPINE TECHNOLOGIES, LLC
SPA-102-022
In Commercial Distribution

  • B030SPA1020220 ()


  • Spinal implant trial
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