SEARCH RESULTS FOR: ("源头企业签名[Contact Telegram: duo785].hfs")(62292 results)

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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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SCR-ON HEM ANG TIB WDG SZ 1-2 30 DEG LT-LA/RT-MD
Smith & Nephew, Inc.
71423029
Not in Commercial Distribution

  • 03596010506290 ()
71423029

  • Knee arthroplasty wedge
SCR-ON HEM ANG TIB WDG SZ 5-6 30 DEG LT-MD/RT-LA
Smith & Nephew, Inc.
71423027
Not in Commercial Distribution

  • 03596010506283 ()
71423027

  • Knee arthroplasty wedge
SCR-ON HEM ANG TIB WDG SZ 3-4 30 DEG LT-MD/RT-LA
Smith & Nephew, Inc.
71423026
Not in Commercial Distribution

  • 03596010506276 ()
71423026

  • Knee arthroplasty wedge
SCR-ON HEM ANG TIB WDG SZ 1-2 30 DEG LT-MD/RT-LA
Smith & Nephew, Inc.
71423025
Not in Commercial Distribution

  • 03596010506269 ()
71423025

  • Knee arthroplasty wedge
SCR-ON HEM ANG TIB WDG SZ 5-6 20 DEG LT-LA/RT-MD
Smith & Nephew, Inc.
71423023
Not in Commercial Distribution

  • 03596010506252 ()
71423023

  • Knee arthroplasty wedge
SCR-ON HEM ANG TIB WDG SZ 3-4 20 DEG LT-LA/RT-MD
Smith & Nephew, Inc.
71423022
Not in Commercial Distribution

  • 03596010506245 ()
71423022

  • Knee arthroplasty wedge
SCR-ON HEM ANG TIB WDG SZ 1-2 20 DEG LT-LA/RT-MD
Smith & Nephew, Inc.
71423021
Not in Commercial Distribution

  • 03596010506238 ()
71423021

  • Knee arthroplasty wedge
SCR-ON HEM ANG TIB WDG SZ 5-6 20 DEG LT-MD/RT-LA
Smith & Nephew, Inc.
71423019
Not in Commercial Distribution

  • 03596010506221 ()
71423019

  • Knee arthroplasty wedge
SCR-ON HEM ANG TIB WDG SZ 3-4 20 DEG LT-MD/RT-LA
Smith & Nephew, Inc.
71423018
Not in Commercial Distribution

  • 03596010506214 ()
71423018

  • Knee arthroplasty wedge
SCR-ON HEM ANG TIB WDG SZ 1-2 20 DEG LT-MD/RT-LA
Smith & Nephew, Inc.
71423017
Not in Commercial Distribution

  • 03596010506207 ()
71423017

  • Knee arthroplasty wedge
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