FDA UDI In Commercial Distribution 🇺🇸 United States

RITLENG PROBE

DI: 13760087126232 · Model: S1.1460 · FCI S A S FCI 20 22
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RITLENG PROBE
Primary DI
13760087126232
Version / Model
S1.1460
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
3
Public Version Date
2023-02-20
Public Version Status
Update
Public Device Record Key
350fb20f-83d9-4a74-917b-53d52bfa8929

Device Description

A hand-held, manual, slender rod-like ophthalmic surgical instrument made of flexible metal, with a blunt bulbous tip, used for exploring the lacrimal canal (the lacrimal duct) during an ophthalmic procedure. This is a reusable device.

Device Characteristics

Single Use
No
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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
OKS Lacrimal Stents And Intubation Sets

GMDN Terms

Code Name
13120 Ophthalmic surgical probe, reusable

Identifiers

Type ID
Primary 13760087126232