FDA UDI In Commercial Distribution 🇺🇸 United States

RITLENG+

DI: 03760087127263 · Model: S1.1455 · FCI S A S FCI 20 22
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
RITLENG+
Primary DI
03760087127263
Version / Model
S1.1455
Company Name
FCI S A S FCI 20 22
Labeler DUNS
763408366
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-30
Public Version
1
Public Version Date
2021-06-07
Public Version Status
New
Public Device Record Key
bcc996da-0e9e-4d55-a88c-23fad921ef26

Device Description

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).

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OKS Lacrimal Stents And Intubation Sets

GMDN Terms

Code Name
17003 Lacrimal tube

Identifiers

Type ID
Package 33760087127264
Primary 03760087127263
Package 13760087127260