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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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HGPII Acetabular Component - 00889024670648

No Description
Zimmer, Inc.
32-6732-90-01
In Commercial Distribution

  • 00889024670648 ()

  • 32 mm I.D. O.D. Size K
32-6732-090-01

  • Non-constrained polyethylene acetabular liner

HGPII Acetabular Component - 00889024670563

No Description
Zimmer, Inc.
32-6732-10-01
In Commercial Distribution

  • 00889024670563 ()

  • 32 mm I.D. O.D. Size K
32-6732-010-01

  • Non-constrained polyethylene acetabular liner

HGPII Acetabular Component - 00889024670464

No Description
Zimmer, Inc.
32-6728-90-01
In Commercial Distribution

  • 00889024670464 ()

  • 28 mm I.D. O.D. Size K
32-6728-090-01

  • Non-constrained polyethylene acetabular liner

HGPII Acetabular Component - 00889024670365

No Description
Zimmer, Inc.
32-6728-10-01
In Commercial Distribution

  • 00889024670365 ()

  • 28 mm I.D. O.D. Size K
32-6728-010-01

  • Non-constrained polyethylene acetabular liner

Medline Industries, Inc. - 10195327646257

PK- K SHOULDER
MEDLINE INDUSTRIES, INC.
DYNJ900034C
In Commercial Distribution

  • 40195327646258 ()
  • 10195327646257 ()
DYNJ900034C

  • General surgical procedure kit, non-medicated, single-use

Medline Industries, Inc. - 10195327575205

DR. K REDDY
MEDLINE INDUSTRIES, INC.
PAIN0828A
In Commercial Distribution

  • 40195327575206 ()
  • 10195327575205 ()
PAIN0828A

  • General surgical procedure kit, non-medicated, single-use

Medline Industries, Inc. - 10889942254354

K KIM ROBOTIC
MEDLINE INDUSTRIES, INC.
DYNJ903070
In Commercial Distribution

  • 10889942254354 ()
DYNJ903070

  • General surgical procedure kit, non-medicated, reusable

Medline Industries, Inc. - 10195327094331

PK- K SHOULDER
MEDLINE INDUSTRIES, INC.
DYNJ900034B
In Commercial Distribution

  • 40195327094332 ()
  • 10195327094331 ()
DYNJ900034B

  • General surgical procedure kit, non-medicated, single-use

NA - 04250869608213

TELIX K Pusher
Biedermann Motech GmbH & Co. KG
209-020-0104
In Commercial Distribution

  • 04250869608213 ()
209-020-0104

  • General internal orthopaedic fixation system implantation kit

NA - 04250869608244

TELIX K Hammer
Biedermann Motech GmbH & Co. KG
209-020-0103
In Commercial Distribution

  • 04250869608244 ()
209-020-0103

  • General internal orthopaedic fixation system implantation kit
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