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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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
RITLENG BICANALICULUS INTUBATION
In Commercial Distribution

  • 33760087120371 ()
  • 03760087120370 ()

  • Length: 300 Millimeter
  • Outer Diameter: 0.64 Millimeter
S1.1450u

  • Lacrimal tube
BIKA® FOR DCR
FCI S A S FCI 20 22
S1.1400
In Commercial Distribution

  • 33760087120357 ()
  • 03760087120356 ()


  • Lacrimal tube
AUTOSTABLE BICANALICULUS INTUBATION SET II (35 MM) WITH DILATOR
FCI S A S FCI 20 22
S1.1392
In Commercial Distribution

  • 13760087120346 ()
  • 03760087120349 ()


  • Lacrimal tube
AUTOSTABLE BICANALICULUS INTUBATION SET II (30 MM) WITH DILATOR
FCI S A S FCI 20 22
S1.1391
In Commercial Distribution

  • 13760087120339 ()
  • 03760087120332 ()


  • Lacrimal tube
AUTOSTABLE BICANALICULUS INTUBATION SET II (25 MM) WITH DILATOR
FCI S A S FCI 20 22
S1.1390
In Commercial Distribution

  • 13760087120322 ()
  • 03760087120325 ()


  • Lacrimal tube
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
CRAWFORD BICANALICULUS INTUBATION
In Commercial Distribution

  • 33760087120234 ()
  • 03760087120233 ()

  • Length: 310 Millimeter
  • Outer Diameter: 0.64 Millimeter
S1.1270u

  • Lacrimal tube
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
INFANT BIKA BICANALICULUS INTUBATION J.A. BERNARD, M.D.
In Commercial Distribution

  • 33760087120173 ()
  • 03760087120172 ()

  • Length: 55 Millimeter
  • Outer Diameter: 0.64 Millimeter
S1.1100

  • Lacrimal tube
BIKA BICANALICULAR INTUBATION SET J.A. BERNARD, M.D.
FCI S A S FCI 20 22
S1.1000
In Commercial Distribution

  • 33760087120104 ()
  • 03760087120103 ()


  • Lacrimal tube
A sterile device inserted into a lacrimal punctum opening to prevent tear outflow in dry eye patients. This is a single-use device.
FCI S A S FCI 20 22
READY-SET PUNCTUM PLUG (MINI, US 0.7)
In Commercial Distribution

  • 23760087120060 ()
  • 03760087120066 ()

  • Outer Diameter: 0.55 Millimeter
S2.3672u

  • Lacrimal punctum plug
ASSIST Silver Absorbent is a sterile, single use multi-layer low-adherent absorbent wound dressing. ASSIST Silver Absorbent is indicated for management of acute and chronic wounds: partial thickness burns, incisions, skin grafts, donor sites, lacerations, abrasions, lymphedema, dermatological wounds, and stage I-IV vascular ulcers, pressure ulcers, venous ulcers, and diabetic ulcers. ASSIST Silver Absorbent dressings provide an antimicrobial barrier and reduces microbial penetration through the dressing. The dressing is contraindicated for patients with a known silver sensitivity. The dressing has a low-adherent veil wound contact layer, a polyester/ nylon wound contact layer coated with an ion-exchange silver, two layers of absorptive non-woven, and a grey occlusive outer layer. The film outer layer (side placed away from the wound) is grey and embossed. The embossing is a circle logo with "ASSIST Silver" printed inside. The logo has "This side away from wound," embossed above and below.
MILLIKEN HEALTHCARE PDTS, LLC
Half Bed 36"x48"
In Commercial Distribution

  • 00015961668626 ()
  • 10015961668623 ()
3000117009

  • Wound-nonadherent dressing, absorbent, antimicrobial
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