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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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Final impactor for cervical cage
SPINEWAY
2
Not in Commercial Distribution

  • 03663422600486 ()
032IC2

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Hook Pusher
SPINEWAY
2
In Commercial Distribution

  • 03663422600455 ()
030IHP2

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Impactor for lumbar cage
SPINEWAY
2
In Commercial Distribution

  • 03663422600370 ()
025HLP2

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Impactor for cervical cage
SPINEWAY
2
Not in Commercial Distribution

  • 03663422600332 ()
022HCP2

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Rod holder
SPINEWAY
2
In Commercial Distribution

  • 03663422600271 ()
018HR2

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Screwdriver, polyaxial
SPINEWAY
2
In Commercial Distribution

  • 03663422600165 ()
011SP2

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Screwdriver, monobloc
SPINEWAY
2
In Commercial Distribution

  • 03663422600141 ()
010SM2

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Module instruments BM
SPINEWAY
2
In Commercial Distribution

  • 03663422500878 ()
M2BM02

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Module implants BM
SPINEWAY
2
In Commercial Distribution

  • 03663422500854 ()
M2BM01

  • Orthopaedic surgical procedure kit, non-medicated, reusable
The AHI System is an adjunctive monitoring method to enable identification of patients who are showing signs of hemodynamic instability or are likely to experience a future episode of hemodynamic instability, and to allow clinicians an opportunity to increase vigilance.
Fifth Eye, Inc.
2
In Commercial Distribution

  • B823AHIV200 ()


  • Clinical management support software
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