Titanium Schepens Forked Retractor

GUDID 00840096207705

KATALYST SURGICAL LLC

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	00840096207705
NIH Device Record Key	05c4d998-42c9-4941-92be-f1eab85b71cc
Commercial Distribution Status	In Commercial Distribution
Brand Name	Titanium Schepens Forked Retractor
Version Model Number	2012
Company DUNS	007883297
Company Name	KATALYST SURGICAL LLC
Device Count	1
DM Exempt	false
Pre-market Exempt	true
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	true
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	00840096207705 [Primary]

FDA Product Code

HNQ	Hook, Ophthalmic