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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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DRILLSAW MAX 600 INSTRUMENT CASE
ARTHREX, INC.
AR-600C-G
In Commercial Distribution

  • 00888867248403 ()
AR-600C-G

  • Device sterilization/disinfection container, reusable
2.9 mm Hip PushLock Disposables Kit
ARTHREX, INC.
AR-2923DHS
In Commercial Distribution

  • 00888867247741 ()
AR-2923DHS

  • Orthopaedic surgical procedure kit, non-medicated, single-use
GUIDE WIRE, THRDED, 2.4 MM X 304 MM, STR
ARTHREX, INC.
AR-8967KT-12S
In Commercial Distribution

  • 00888867247147 ()
AR-8967KT-12S

  • Fluted surgical drill bit, single-use
GUIDE WIRE, THRDED, 2.4 MM X 203 MM, STR
ARTHREX, INC.
AR-8967KTS
In Commercial Distribution

  • 00888867247130 ()
AR-8967KTS

  • Fluted surgical drill bit, single-use
GUIDE WIRE, 2.4 MM X 304 MM, STRL
ARTHREX, INC.
AR-8967K-12S
In Commercial Distribution

  • 00888867247123 ()
AR-8967K-12S

  • Fluted surgical drill bit, single-use
GUIDE WIRE, 2.4 MM X 203 MM, STRL
ARTHREX, INC.
AR-8967KS
In Commercial Distribution

  • 00888867247116 ()
AR-8967KS

  • Suturing unit, single-use
GUIDE WIRE, 2 MM X 203 MM, STRL
ARTHREX, INC.
AR-8956K-01S
In Commercial Distribution

  • 00888867247109 ()
AR-8956K-01S

  • Suturing unit, single-use
SCHANZ PIN, 5.0MM, STRL
ARTHREX, INC.
AR-8954-01S
In Commercial Distribution

  • 00888867247093 ()
AR-8954-01S

  • Suturing unit, single-use
GUIDE WIRE, DOUBLE TROCAR, 1.14 MM, STRL
ARTHREX, INC.
AR-8950-06S
In Commercial Distribution

  • 00888867247086 ()
AR-8950-06S

  • Fluted surgical drill bit, single-use
GUIDE WIRE, 2 MM X 150 MM, STRL.
ARTHREX, INC.
AR-8945KS
In Commercial Distribution

  • 00888867247079 ()
AR-8945KS

  • Suturing unit, single-use
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