SEARCH RESULTS FOR: 代办AT(7976 results)

Export results
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

Show Filters

Hyalgan® Sodium Hylauronate (20mg/2mL) in the 2mL vial is indicated for the treatment of pain in osteoarthritis (OA) of the knee in patients who have failed to respond adequately to conservative nonpharmacologic therapy and to simple analgesics, e.g., acetaminophen. It is a viscous solution of purified natural Sodium Hylauronate (Hyalectin®) in buffered physiological sodium chloride. The sodium hylauronate is extracted from rooster combs. It is given by intra-articular injection in a treatment cycle consisting of five injections given at weekly intervals. Some patients may experience benefit with three injections given at weekly cycles. This has been noted in studies reported in the literature in which patients treated with three injections were followed for 60 days.
FIDIA FARMACEUTICI SPA
89122-0724-12
Not in Commercial Distribution

  • M71389122072412A1 ()
89122-0724-12

  • Synovial fluid supplementation medium
Hyalgan® Sodium Hylauronate (20mg/2mL) in the 2mL vial is indicated for the treatment of pain in osteoarthritis (OA) of the knee in patients who have failed to respond adequately to conservative nonpharmacologic therapy and to simple analgesics, e.g., acetaminophen. It is a viscous solution of purified natural Sodium Hylauronate (Hyalectin®) in buffered physiological sodium chloride. The sodium hylauronate is extracted from rooster combs. It is given by intra-articular injection in a treatment cycle consisting of five injections given at weekly intervals. Some patients may experience benefit with three injections given at weekly cycles. This has been noted in studies reported in the literature in which patients treated with three injections were followed for 60 days.
FIDIA FARMACEUTICI SPA
89122-0724-12
In Commercial Distribution

89122-0724-12

  • Synovial fluid supplementation medium
BTM Light Weight Monitoring Defib Module
BOUND TREE MEDICAL, LLC
2525-61323
In Commercial Distribution

  • 00815277020664 ()


  • Blood pressure cuff, reusable
  • Transcutaneous blood gas monitor sensor
  • Intracardiac oximeter
  • General-purpose patient temperature probe, single-use
Absolute Pro Vascular Self-Expanding Stent System 10.0 mm x 100 mm x 135 cm / Over-The-Wire
ABBOTT VASCULAR INC.
1012538-100
In Commercial Distribution

  • 08717648176319 ()
1012538-100

  • Peripheral artery stent, bare-metal
Absolute Pro Vascular Self-Expanding Stent System 10.0 mm x 80 mm x 135 cm / Over-The-Wire
ABBOTT VASCULAR INC.
1012538-80
In Commercial Distribution

  • 08717648176302 ()
1012538-80

  • Peripheral artery stent, bare-metal
Absolute Pro Vascular Self-Expanding Stent System 10.0 mm x 60 mm x 135 cm / Over-The-Wire
ABBOTT VASCULAR INC.
1012538-60
In Commercial Distribution

  • 08717648176296 ()
1012538-60

  • Peripheral artery stent, bare-metal
Absolute Pro Vascular Self-Expanding Stent System 10.0 mm x 40 mm x 135 cm / Over-The-Wire
ABBOTT VASCULAR INC.
1012538-40
In Commercial Distribution

  • 08717648176289 ()
1012538-40

  • Peripheral artery stent, bare-metal
Absolute Pro Vascular Self-Expanding Stent System 10.0 mm x 30 mm x 135 cm / Over-The-Wire
ABBOTT VASCULAR INC.
1012538-30
In Commercial Distribution

  • 08717648176272 ()
1012538-30

  • Peripheral artery stent, bare-metal
Absolute Pro Vascular Self-Expanding Stent System 10.0 mm x 20 mm x 135 cm / Over-The-Wire
ABBOTT VASCULAR INC.
1012538-20
In Commercial Distribution

  • 08717648176265 ()
1012538-20

  • Peripheral artery stent, bare-metal
Absolute Pro Vascular Self-Expanding Stent System 9.0 mm x 100 mm x 135 cm/ Over-The-Wire
ABBOTT VASCULAR INC.
1012537-100
In Commercial Distribution

  • 08717648176258 ()
1012537-100

  • Peripheral artery stent, bare-metal
< 1 ... 586 587 588 589 590 ... 798 >