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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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Stride Femur Size 5 RM/LL
Smith & Nephew, Inc.
PFSI00060
In Commercial Distribution

  • 00885556626658 ()
PFSI00060

  • Uncoated unicondylar knee femur prosthesis
Stride Femur Size 5 LM/RL
Smith & Nephew, Inc.
PFSI00059
In Commercial Distribution

  • 00885556626573 ()
PFSI00059

  • Uncoated unicondylar knee femur prosthesis
JAR W LID 10ML 5 KIT
Cardinal Health 200, LLC
07B6667B
In Commercial Distribution

  • 50197106042555 ()
  • 10197106042557 ()
07B6667B

  • General surgical procedure kit, non-medicated, single-use
Vivacit-E Articular Surface Size 5 14mm
Smith & Nephew, Inc.
00584209514
In Commercial Distribution

  • 00885556621103 ()
00584209514

  • Unicondylar knee insert
Vivacit-E Articular Surface Size 5 12mm
Smith & Nephew, Inc.
00584209512
In Commercial Distribution

  • 00885556621097 ()
00584209512

  • Unicondylar knee insert
Vivacit-E Articular Surface Size 5 11mm
Smith & Nephew, Inc.
00584209511
In Commercial Distribution

  • 00885556621080 ()
00584209511

  • Unicondylar knee insert
Vivacit-E Articular Surface Size 5 10mm
Smith & Nephew, Inc.
00584209510
In Commercial Distribution

  • 00885556621073 ()
00584209510

  • Unicondylar knee insert
Vivacit-E Articular Surface Size 5 9mm
Smith & Nephew, Inc.
00584209509
In Commercial Distribution

  • 00885556621066 ()
00584209509

  • Unicondylar knee insert
Vivacit-E Articular Surface Size 5 8mm
Smith & Nephew, Inc.
00584209508
In Commercial Distribution

  • 00885556621059 ()
00584209508

  • Unicondylar knee insert
TRUEPASS DISPOSABLE NEEDLES 5 PER BOX
Smith & Nephew, Inc.
72203793
In Commercial Distribution

  • 00885554030433 ()
  • 20885554030437 ()
72203793

  • Suturing needle, single-use
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