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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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Acellular fish skin for topical and surgical wounds. INTENDED USE Kerecis® Burn is indicated for the management of wounds including: - Partial and full-thickness wounds, - Trauma wounds (abrasions, lacerations, second-degree burns, skin tears). Pentagon Meshed Double Pouched https://www.kerecis.com/wp-content/uploads/2020/10/A5-KM-19-0146-IFU-Kerecis-Burn-US.pdf
KERECIS hf.
250cm2 Meshed Burn
In Commercial Distribution

  • 05694310960670 ()
  • 05694310960687 ()

  • Length: 250 Centimeter
  • Width: 250 Centimeter
50202M24D0D

  • Animal-derived wound matrix dressing
No Description
CRAWFORD HEALTHCARE LIMITED
16 x 16in
In Commercial Distribution

  • 05060077233706 ()
  • 05060077233690 ()
  • 05060077233683 ()

  • Length: 16 Inch
  • Height: 16 Inch
CWL1163

  • Exudate-absorbent dressing, hydrophilic-gel, antimicrobial
BURNSHIELD DRESSING 50MMX1M (2X40") LIMB
BURNSHIELD (PTY) LTD
901131
In Commercial Distribution

  • 16007645001424 ()
  • 06007645001427 ()
  • 26007645001421 ()

  • Length: 1000 Millimeter
  • Width: 50 Millimeter
  • Weight: 150 Gram
901131

  • Synthetic polymer burn dressing, gel-coated
AMD Antimicrobial Fenestrated Foam Disc Dressing,0.5% Polyhexamethylene Biguanide HCI (PHMB)
Cardinal Health, Inc.
55512AMDX
In Commercial Distribution

  • 00884521065577 ()
  • 10884521065543 ()
  • 00884521065546 ()

  • Outer Diameter: 0.25 Inch
  • Outer Diameter: 1 Inch
55512AMDX

  • Wound-nonadherent dressing, absorbent, antimicrobial
A sterile, implantable, single-lumen tube intended to provide tear drainage from the front surface of the eye, typically into the nasal cavity or a paranasal sinus, as a drainage treatment for lacrimal canalicular pathologies in functional or obstructive epiphora; it may also be intended to facilitate saline solution irrigation to a paranasal sinus (e.g., ethmoid sinus) to manage chronic rhinosinusitis. Also referred to as a lacrimal stent, the device may be implanted after surgery to dilate or create a surgical passage [e.g., dacryocystostomy/dacryocystorhinostomy (DCR)], and is made of glass or synthetic polymer material(s) [e.g., silicone].
FCI S A S FCI 20 22
MINI MONOKA ® FAYET & BERNARD ®
In Commercial Distribution

  • 33760087120395 ()
  • 03760087120394 ()

  • Length: 50 Millimeter
S1.1500

  • Lacrimal tube
StopsBleeding™ 10g pouch
Coag Medical, LLC
SBP0010
In Commercial Distribution

  • 00850817006456 ()


  • Plant polysaccharide haemostatic agent, bioabsorbable
BleedStop™ 150g pouch
Coag Medical, LLC
BSP0150
In Commercial Distribution

  • 00850817006326 ()


  • Plant polysaccharide haemostatic agent, bioabsorbable
Box of 4 BleedStop™ 15g pouches
Coag Medical, LLC
BSP0415
In Commercial Distribution

  • 00850817006265 ()


  • Plant polysaccharide haemostatic agent, bioabsorbable
BleedStop™ 20g pouch
Coag Medical, LLC
BSP0020
In Commercial Distribution

  • 00850817006258 ()


  • Plant polysaccharide haemostatic agent, bioabsorbable
BleedStop™ 60g pouch
Coag Medical, LLC
BSP0060
In Commercial Distribution

  • 00850817006241 ()


  • Plant polysaccharide haemostatic agent, bioabsorbable
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