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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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iBALANCE UKA, TIBIAL ALIGNMENT GUIDE
ARTHREX, INC.
AR-601-TG00
In Commercial Distribution

  • 00888867037830 ()
AR-601-TG00

  • Suturing unit, single-use
IBAL UKA,POST RESECT GD,10MM
ARTHREX, INC.
AR-601-PB10
In Commercial Distribution

  • 00888867037311 ()
AR-601-PB10

  • Suturing unit, single-use
IBAL UKA,POST RESECT GD,9MM
ARTHREX, INC.
AR-601-PB09
In Commercial Distribution

  • 00888867037304 ()
AR-601-PB09

  • Suturing unit, single-use
IBAL UKA,POST RESECT GD,8MM
ARTHREX, INC.
AR-601-PB08
In Commercial Distribution

  • 00888867037298 ()
AR-601-PB08

  • Suturing unit, single-use
IBAL UKA,POST RESCTION GD,7MM
ARTHREX, INC.
AR-601-PB07
In Commercial Distribution

  • 00888867037281 ()
AR-601-PB07

  • Suturing unit, single-use
IBAL UKA,POST RESECT GD,6MM
ARTHREX, INC.
AR-601-PB06
In Commercial Distribution

  • 00888867037274 ()
AR-601-PB06

  • Suturing unit, single-use
IBAL UKA,POST RESECT GD,5MM
ARTHREX, INC.
AR-601-PB05
In Commercial Distribution

  • 00888867037267 ()
AR-601-PB05

  • Suturing unit, single-use
IBAL UKA,POST RESECT GD,4MM
ARTHREX, INC.
AR-601-PB04
In Commercial Distribution

  • 00888867037250 ()
AR-601-PB04

  • Suturing unit, single-use
IBAL UKA,POST RESECT GD,3MM
ARTHREX, INC.
AR-601-PB03
In Commercial Distribution

  • 00888867037243 ()
AR-601-PB03

  • Suturing unit, single-use
IBAL UKA,CHAMFER & PEG GD,SZ 6,RM/LL
ARTHREX, INC.
AR-601-CRMF
In Commercial Distribution

  • 00888867036994 ()
AR-601-CRMF

  • Arthroscopic shaver system blade, reusable
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