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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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Liner, 36-52/54mm (20° Hood)
ORTHOMEDFLEX LLC
111120652
In Commercial Distribution

  • M7161111206520 ()
111-12-0652

  • Non-constrained polyethylene acetabular liner
Liner, 40-60/68mm (20° Hood)
ORTHOMEDFLEX LLC
111120460
In Commercial Distribution

  • M7161111204600 ()
111-12-0460

  • Non-constrained polyethylene acetabular liner
Liner, 40-56/58mm (20° Hood)
ORTHOMEDFLEX LLC
111120456
In Commercial Distribution

  • M7161111204560 ()
111-12-0456

  • Non-constrained polyethylene acetabular liner
Liner, 32-60/68mm (20° Hood)
ORTHOMEDFLEX LLC
111120260
In Commercial Distribution

  • M7161111202600 ()
111-12-0260

  • Non-constrained polyethylene acetabular liner
Liner, 32-56/58mm (20° Hood)
ORTHOMEDFLEX LLC
111120256
In Commercial Distribution

  • M7161111202560 ()
111-12-0256

  • Non-constrained polyethylene acetabular liner
Liner, 32-52/54mm (20° Hood)
ORTHOMEDFLEX LLC
111120252
In Commercial Distribution

  • M7161111202520 ()
111-12-0252

  • Non-constrained polyethylene acetabular liner
Liner, 32-48/50mm (20° Hood)
ORTHOMEDFLEX LLC
111120250
In Commercial Distribution

  • M7161111202500 ()
111-12-0250

  • Non-constrained polyethylene acetabular liner
5:20 Pm Brown Spectacle
Kenmark Optical, Inc.
520PBR60
In Commercial Distribution

  • 00715317196246 ()


  • Prescription spectacles
5:20 Pm Brown Spectacle
Kenmark Optical, Inc.
520PBR58
In Commercial Distribution

  • 00715317196239 ()


  • Prescription spectacles
5:20 Pm Brown Spectacle
Kenmark Optical, Inc.
520PBR56
In Commercial Distribution

  • 00715317196222 ()


  • Prescription spectacles
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