RITLENG PROBE

GUDID 13760087126232

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.

FCI S A S FCI 20 22

Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable

Primary Device ID	13760087126232
NIH Device Record Key	350fb20f-83d9-4a74-917b-53d52bfa8929
Commercial Distribution Status	In Commercial Distribution
Brand Name	RITLENG PROBE
Version Model Number	S1.1460
Company DUNS	763408366
Company Name	FCI S A S FCI 20 22
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	false
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	13760087126232 [Primary]

FDA Product Code

OKS	Lacrimal Stents And Intubation Sets