RITLENG+ PVP - An implantable short tube intended to provide a - FCI S A S FCI 20 22

Duns Number:763408366

Device Description: An implantable short tube intended to provide a bypass route for tear drainage from the co An implantable short tube intended to provide a bypass route for tear drainage from the corner of the eye into the nasal cavity, or a paranasal sinus, as treatment for pathologies of the tear drainage system in association with 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 (e.g., Lester Jones type), it is implanted after surgery to dilate or maintain a surgically-created passage [e.g., dacryocystostomy/dacryocystorhinostomy (DCR)], and is made of glass or synthetic polymer materials (e.g., silicone).

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More Product Details

Catalog Number

-

Brand Name

RITLENG+ PVP

Version/Model Number

S1.1495

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

OKS

Product Code Name

Lacrimal Stents And Intubation Sets

Device Record Status

Public Device Record Key

94832746-af6e-4d4c-b080-a613f4b875a4

Public Version Date

June 07, 2021

Public Version Number

1

DI Record Publish Date

May 30, 2021

Additional Identifiers

Package DI Number

33760087127271

Quantity per Package

3

Contains DI Package

03760087127270

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-

"FCI S A S FCI 20 22" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 82
2 A medical device with a moderate to high risk that requires special controls. 291
U Unclassified 60