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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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StarPore Patient Specific Implant
ANATOMICS PTY LTD
CI-STARPORE-OT
In Commercial Distribution

  • 09349797001700 ()
CI-STARPORE-OT

  • Polyethylene craniofacial tissue reconstructive material
StarPore Patient Specific Implant (Other)
ANATOMICS PTY LTD
CI-STARPORE-O
In Commercial Distribution

  • 09349797000239 ()
CI-STARPORE-O

  • Polyethylene craniofacial tissue reconstructive material
StarPore Patient Specific Implant (X-Large)
ANATOMICS PTY LTD
CI-STARPORE-XL
In Commercial Distribution

  • 09349797000222 ()
CI-STARPORE-XL

  • Polyethylene craniofacial tissue reconstructive material
StarPore Patient Specific Implant (Large)
ANATOMICS PTY LTD
CI-STARPORE-L
In Commercial Distribution

  • 09349797000215 ()
CI-STARPORE-L

  • Polyethylene craniofacial tissue reconstructive material
StarPore Patient Specific Implant (Medium)
ANATOMICS PTY LTD
CI-STARPORE-M
In Commercial Distribution

  • 09349797000208 ()
CI-STARPORE-M

  • Polyethylene craniofacial tissue reconstructive material
StarPore Patient Specific Implant (Small)
ANATOMICS PTY LTD
CI-STARPORE-S
In Commercial Distribution

  • 09349797000192 ()
CI-STARPORE-S

  • Polyethylene craniofacial tissue reconstructive material
No Description
SIGNATURE ORTHOPAEDICS PTY LTD
121-20-8630
In Commercial Distribution

  • 09348215139285 ()


  • Polyethylene patella prosthesis
No Description
SIGNATURE ORTHOPAEDICS PTY LTD
121-20-8530
In Commercial Distribution

  • 09348215139278 ()


  • Polyethylene patella prosthesis
No Description
SIGNATURE ORTHOPAEDICS PTY LTD
121-20-8430
In Commercial Distribution

  • 09348215139261 ()


  • Polyethylene patella prosthesis
No Description
SIGNATURE ORTHOPAEDICS PTY LTD
121-20-8230
In Commercial Distribution

  • 09348215139254 ()


  • Polyethylene patella prosthesis
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