FDA UDI In Commercial Distribution 🇺🇸 United States

LACRIFLOW CL

DI: 04540778171381 · Model: LF-CL105A · KANEKA CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
LACRIFLOW CL
Primary DI
04540778171381
Version / Model
LF-CL105A
Company Name
KANEKA CORPORATION
Labeler DUNS
690535406
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-01
Public Version
6
Public Version Date
2023-09-11
Public Version Status
Update
Public Device Record Key
edd4ddd2-41a4-47cf-8730-7b6cfe7bc899

Device Description

The Lacriflow CL is indicated in treatments of epiphora in patients 12 months and older, in cases of: - Canalicular pathologies (stenosis, obstruction, lacerations), - During Dacryocystorhinostomy (conventional or laser), - Congenital nasolacrimal duct obstruction.

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
Primary 04540778171381
Package 14540778171388

Customer Contacts

Phone
800-526-3522

Device Sizes

Type Value Unit Text
Length 105 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store the LACRIFLOW CL in the place avoiding direct sunlight at room temperature.